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dbVar

Database of genomic structural variation

nsv5648751

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: 340 SVs from 56 studies. See in: genome view

Submitted genomic17,132,531-17,132,531

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5648751	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	17,132,531	17,132,531
nsv5648751	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	17,226,388	17,226,388

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17093523	insertion	HG03065	Sequencing	Sequence alignment	3,836

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17093523	Submitted genomic		NC_000016.10:g.171 32531_17132532ins6 1	GRCh38 (hg38)		NC_000016.10	Chr16	17,132,531	17,132,531
nssv17093523	Remapped	Perfect	NC_000016.9:g.1722 6388_17226389ins61	GRCh37.p13	First Pass	NC_000016.9	Chr16	17,226,388	17,226,388

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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