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dbVar

Database of genomic structural variation

nsv5637977

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: 217 SVs from 43 studies. See in: genome view

Submitted genomic55,911,102-55,911,102

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5637977	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	55,911,102	55,911,102
nsv5637977	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	56,823,661	56,823,661

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17147907	insertion	NA12329	Sequencing	Sequence alignment	1,517

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17147907	Submitted genomic		NC_000008.11:g.559 11102_55911103ins6 1	GRCh38 (hg38)		NC_000008.11	Chr8	55,911,102	55,911,102
nssv17147907	Remapped	Perfect	NC_000008.10:g.568 23661_56823662ins6 1	GRCh37.p13	First Pass	NC_000008.10	Chr8	56,823,661	56,823,661

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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