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dbVar

Database of genomic structural variation

nsv5618541

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: 113 SVs from 26 studies. See in: genome view

Submitted genomic126,783,743-126,783,743

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5618541	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	126,783,743	126,783,743
nsv5618541	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	126,502,586	126,502,586

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17126479	insertion	HG03371	Sequencing	Sequence alignment	2,852

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17126479	Submitted genomic		NC_000003.12:g.126 783743_126783744in s318	GRCh38 (hg38)		NC_000003.12	Chr3	126,783,743	126,783,743
nssv17126479	Remapped	Perfect	NC_000003.11:g.126 502586_126502587in s318	GRCh37.p13	First Pass	NC_000003.11	Chr3	126,502,586	126,502,586

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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