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dbVar

Database of genomic structural variation

nsv5643527

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 88 SVs from 21 studies. See in: genome view

Submitted genomic173,067,531-173,067,531

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5643527	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	173,067,531	173,067,531
nsv5643527	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	172,494,534	172,494,534

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17122188	insertion	SAMN00249812	Sequencing	Sequence alignment	1,255

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17122188	Submitted genomic		NC_000005.10:g.173 067531_173067532in s3801	GRCh38 (hg38)		NC_000005.10	Chr5	173,067,531	173,067,531
nssv17122188	Remapped	Perfect	NC_000005.9:g.1724 94534_172494535ins 3801	GRCh37.p13	First Pass	NC_000005.9	Chr5	172,494,534	172,494,534

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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