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dbVar

Database of genomic structural variation

nsv5653055

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: 195 SVs from 15 studies. See in: genome view

Submitted genomic46,546,293-46,546,293

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5653055	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	46,546,293	46,546,293
nsv5653055	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	44,126,256	44,126,256

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17101462	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
nssv17101462	Submitted genomic		NC_000018.10:g.465 46293_46546294ins1 01	GRCh38 (hg38)		NC_000018.10	Chr18	46,546,293	46,546,293
nssv17101462	Remapped	Perfect	NC_000018.9:g.4412 6256_44126257ins10 1	GRCh37.p13	First Pass	NC_000018.9	Chr18	44,126,256	44,126,256

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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