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dbVar

Database of genomic structural variation

nsv5636883

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: 109 SVs from 28 studies. See in: genome view

Submitted genomic44,883,774-44,883,774

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5636883	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	44,883,774	44,883,774
nsv5636883	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	44,923,373	44,923,373

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17154452	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
nssv17154452	Submitted genomic		NC_000007.14:g.448 83774_44883775ins5 4	GRCh38 (hg38)		NC_000007.14	Chr7	44,883,774	44,883,774
nssv17154452	Remapped	Perfect	NC_000007.13:g.449 23373_44923374ins5 4	GRCh37.p13	First Pass	NC_000007.13	Chr7	44,923,373	44,923,373

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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