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dbVar

Database of genomic structural variation

nsv5627464

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: 377 SVs from 48 studies. See in: genome view

Submitted genomic10,640,009-10,640,009

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5627464	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	10,640,009	10,640,009
nsv5627464	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	10,640,121	10,640,121

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17119927	insertion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17119927	Submitted genomic		NC_000005.10:g.106 40009_10640010ins1 56	GRCh38 (hg38)		NC_000005.10	Chr5	10,640,009	10,640,009
nssv17119927	Remapped	Perfect	NC_000005.9:g.1064 0121_10640122ins15 6	GRCh37.p13	First Pass	NC_000005.9	Chr5	10,640,121	10,640,121

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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