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dbVar

Database of genomic structural variation

nsv5625385

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: 1078 SVs from 79 studies. See in: genome view

Submitted genomic39,385,657-39,385,657

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5625385	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	39,385,657	39,385,657
nsv5625385	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	39,243,176	39,243,176

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17154237	insertion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17154237	Submitted genomic		NC_000008.11:g.393 85657_39385658ins1 28	GRCh38 (hg38)		NC_000008.11	Chr8	39,385,657	39,385,657
nssv17154237	Remapped	Perfect	NC_000008.10:g.392 43176_39243177ins1 28	GRCh37.p13	First Pass	NC_000008.10	Chr8	39,243,176	39,243,176

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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