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dbVar

Database of genomic structural variation

nsv5605006

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

Submitted genomic171,013,719-171,013,719

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5605006	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	171,013,719	171,013,719
nsv5605006	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	170,731,508	170,731,508

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17124330	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17124330	Submitted genomic		NC_000003.12:g.171 013719_171013720in s169	GRCh38 (hg38)		NC_000003.12	Chr3	171,013,719	171,013,719
nssv17124330	Remapped	Perfect	NC_000003.11:g.170 731508_170731509in s169	GRCh37.p13	First Pass	NC_000003.11	Chr3	170,731,508	170,731,508

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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