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dbVar

Database of genomic structural variation

nsv5658361

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

Submitted genomic97,456,698-97,456,698

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5658361	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	97,456,698	97,456,698
nsv5658361	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	98,108,952	98,108,952

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17092201	insertion	HG02818	Sequencing	Sequence alignment	3,473

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17092201	Submitted genomic		NC_000013.11:g.974 56698_97456699ins2 87	GRCh38 (hg38)		NC_000013.11	Chr13	97,456,698	97,456,698
nssv17092201	Remapped	Perfect	NC_000013.10:g.981 08952_98108953ins2 87	GRCh37.p13	First Pass	NC_000013.10	Chr13	98,108,952	98,108,952

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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