Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

Please click here to confirm download.

Supporting Variant Placements for nstd193
Study ID	Variant ID	Variant Region type	Variant Call type	Sampleset ID	Method	Analysis ID	Validation	Variant samples	Subject phenotype	Clinical Interpretation	Assembly	Accession	Chr	Outer-Start	Start	Inner-Start	Inner-End	End	Outer-End	Placement Type	Remap Score
nstd193	nssv16215102		deletion		Sequencing	Read depth and paired-end mapping	Yes	7119_PCDHA			GRCh37 (hg19)	NC_000005.9	5	140214374		140215019	140228422		140229049	Submitted genomic
nstd193	nssv16215102		deletion		Sequencing	Read depth and paired-end mapping	Yes	7119_PCDHA			GRCh37 (hg19)	NC_000005.9	5	140214374		140215019	140228422		140229049	Submitted genomic
nstd193	nssv16215102		deletion		Sequencing	Read depth and paired-end mapping	Yes	7119_PCDHA			GRCh38.p12	NC_000005.10	5	140834789		140835434	140848837		140849464	Remapped	1
nstd193	nssv16215103		deletion		Sequencing	Read depth and paired-end mapping	Yes	7408_PCDHA			GRCh37 (hg19)	NC_000005.9	5	140214374		140215019	140228422		140229049	Submitted genomic
nstd193	nssv16215103		deletion		Sequencing	Read depth and paired-end mapping	Yes	7408_PCDHA			GRCh37 (hg19)	NC_000005.9	5	140214374		140215019	140228422		140229049	Submitted genomic
nstd193	nssv16215103		deletion		Sequencing	Read depth and paired-end mapping	Yes	7408_PCDHA			GRCh38.p12	NC_000005.10	5	140834789		140835434	140848837		140849464	Remapped	1
nstd193	nssv16215104		deletion		Sequencing	Read depth and paired-end mapping	Yes	7432_PCDHA			GRCh37 (hg19)	NC_000005.9	5	140214374		140215019	140228422		140229049	Submitted genomic
nstd193	nssv16215104		deletion		Sequencing	Read depth and paired-end mapping	Yes	7432_PCDHA			GRCh37 (hg19)	NC_000005.9	5	140214374		140215019	140228422		140229049	Submitted genomic
nstd193	nssv16215104		deletion		Sequencing	Read depth and paired-end mapping	Yes	7432_PCDHA			GRCh38.p12	NC_000005.10	5	140834789		140835434	140848837		140849464	Remapped	1
nstd193	nssv16215105		deletion		Sequencing	Read depth and paired-end mapping	Yes	7592_PCDHA			GRCh37 (hg19)	NC_000005.9	5	140214374		140215019	140228422		140229049	Submitted genomic
nstd193	nssv16215105		deletion		Sequencing	Read depth and paired-end mapping	Yes	7592_PCDHA			GRCh37 (hg19)	NC_000005.9	5	140214374		140215019	140228422		140229049	Submitted genomic
nstd193	nssv16215105		deletion		Sequencing	Read depth and paired-end mapping	Yes	7592_PCDHA			GRCh38.p12	NC_000005.10	5	140834789		140835434	140848837		140849464	Remapped	1
nstd193	nssv16215106		deletion		Sequencing	Read depth and paired-end mapping	Yes	7693_PCDHA			GRCh37 (hg19)	NC_000005.9	5	140214374		140215019	140228422		140229049	Submitted genomic
nstd193	nssv16215106		deletion		Sequencing	Read depth and paired-end mapping	Yes	7693_PCDHA			GRCh37 (hg19)	NC_000005.9	5	140214374		140215019	140228422		140229049	Submitted genomic
nstd193	nssv16215106		deletion		Sequencing	Read depth and paired-end mapping	Yes	7693_PCDHA			GRCh38.p12	NC_000005.10	5	140834789		140835434	140848837		140849464	Remapped	1

You are here: NCBI