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dbVar

Database of genomic structural variation

nsv5635353

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: 190 SVs from 29 studies. See in: genome view

Submitted genomic37,808,524-37,808,524

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5635353	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	37,808,524	37,808,524
nsv5635353	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	37,808,521	37,808,521

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17162169	insertion	NA24385	Sequencing	Sequence alignment	2,573

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17162169	Submitted genomic		NC_000009.12:g.378 08524_37808525ins6 0	GRCh38 (hg38)		NC_000009.12	Chr9	37,808,524	37,808,524
nssv17162169	Remapped	Perfect	NC_000009.11:g.378 08521_37808522ins6 0	GRCh37.p13	First Pass	NC_000009.11	Chr9	37,808,521	37,808,521

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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