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dbVar

Database of genomic structural variation

nsv5611375

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: 157 SVs from 33 studies. See in: genome view

Submitted genomic140,997,688-140,997,688

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5611375	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	140,997,688	140,997,688
nsv5611375	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	141,918,842	141,918,842

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17133256	insertion	SAMN00016965	Sequencing	Sequence alignment	1,475

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17133256	Submitted genomic		NC_000004.12:g.140 997688_140997689in s57	GRCh38 (hg38)		NC_000004.12	Chr4	140,997,688	140,997,688
nssv17133256	Remapped	Perfect	NC_000004.11:g.141 918842_141918843in s57	GRCh37.p13	First Pass	NC_000004.11	Chr4	141,918,842	141,918,842

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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