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dbVar

Database of genomic structural variation

nsv5607946

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: 129 SVs from 24 studies. See in: genome view

Submitted genomic86,674,895-86,674,895

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5607946	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	86,674,895	86,674,895
nsv5607946	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	87,140,578	87,140,578

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17066549	insertion	HG03683	Sequencing	Sequence alignment	2,232

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17066549	Submitted genomic		NC_000001.11:g.866 74895_86674896ins6 053	GRCh38 (hg38)		NC_000001.11	Chr1	86,674,895	86,674,895
nssv17066549	Remapped	Perfect	NC_000001.10:g.871 40578_87140579ins6 053	GRCh37.p13	First Pass	NC_000001.10	Chr1	87,140,578	87,140,578

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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