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dbVar

Database of genomic structural variation

nsv5642900

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: 111 SVs from 33 studies. See in: genome view

Submitted genomic42,704,251-42,704,251

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5642900	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	42,704,251	42,704,251
nsv5642900	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	43,199,699	43,199,699

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17070034	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
nssv17070034	Submitted genomic		NC_000010.11:g.427 04251_42704252ins5 1	GRCh38 (hg38)		NC_000010.11	Chr10	42,704,251	42,704,251
nssv17070034	Remapped	Perfect	NC_000010.10:g.431 99699_43199700ins5 1	GRCh37.p13	First Pass	NC_000010.10	Chr10	43,199,699	43,199,699

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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