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dbVar

Database of genomic structural variation

nsv5568978

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:58

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: 1292 SVs from 84 studies. See in: genome view

Submitted genomic39,415,091-39,415,148

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5568978	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	39,415,091	39,415,148
nsv5568978	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	39,272,610	39,272,667

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17143786	deletion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17143786	Submitted genomic		NC_000008.11:g.394 15091_39415148delC	GRCh38 (hg38)		NC_000008.11	Chr8	39,415,091	39,415,148
nssv17143786	Remapped	Perfect	NC_000008.10:g.392 72610_39272667delC	GRCh37.p13	First Pass	NC_000008.10	Chr8	39,272,610	39,272,667

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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