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dbVar

Database of genomic structural variation

nsv5610648

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: 235 SVs from 58 studies. See in: genome view

Submitted genomic21,986,212-21,986,212

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5610648	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	21,986,212	21,986,212
nsv5610648	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	22,312,705	22,312,705

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17062734	insertion	HG01505	Sequencing	Sequence alignment	1,109

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17062734	Submitted genomic		NC_000001.11:g.219 86212_21986213ins3 06	GRCh38 (hg38)		NC_000001.11	Chr1	21,986,212	21,986,212
nssv17062734	Remapped	Perfect	NC_000001.10:g.223 12705_22312706ins3 06	GRCh37.p13	First Pass	NC_000001.10	Chr1	22,312,705	22,312,705

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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