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dbVar

Database of genomic structural variation

nsv5623863

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

Submitted genomic137,885,796-137,885,796

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5623863	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	137,885,796	137,885,796
nsv5623863	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	138,643,366	138,643,366

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17109251	insertion	SAMN00007882	Sequencing	Sequence alignment	1,354

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17109251	Submitted genomic		NC_000002.12:g.137 885796_137885797in s1324	GRCh38 (hg38)		NC_000002.12	Chr2	137,885,796	137,885,796
nssv17109251	Remapped	Perfect	NC_000002.11:g.138 643366_138643367in s1324	GRCh37.p13	First Pass	NC_000002.11	Chr2	138,643,366	138,643,366

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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