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dbVar

Database of genomic structural variation

nsv5646374

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: 116 SVs from 25 studies. See in: genome view

Submitted genomic75,709,974-75,709,974

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5646374	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	75,709,974	75,709,974
nsv5646374	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	76,176,317	76,176,317

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17083017	insertion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17083017	Submitted genomic		NC_000014.9:g.7570 9974_75709975ins31 4	GRCh38 (hg38)		NC_000014.9	Chr14	75,709,974	75,709,974
nssv17083017	Remapped	Perfect	NC_000014.8:g.7617 6317_76176318ins31 4	GRCh37.p13	First Pass	NC_000014.8	Chr14	76,176,317	76,176,317

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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