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dbVar

Database of genomic structural variation

nsv5644335

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: 92 SVs from 22 studies. See in: genome view

Submitted genomic42,834,618-42,834,618

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5644335	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	42,834,618	42,834,618
nsv5644335	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	43,330,066	43,330,066

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17070040	insertion	HG02011	Sequencing	Sequence alignment	2,906

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17070040	Submitted genomic		NC_000010.11:g.428 34618_42834619ins3 19	GRCh38 (hg38)		NC_000010.11	Chr10	42,834,618	42,834,618
nssv17070040	Remapped	Perfect	NC_000010.10:g.433 30066_43330067ins3 19	GRCh37.p13	First Pass	NC_000010.10	Chr10	43,330,066	43,330,066

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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