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dbVar

Database of genomic structural variation

nsv5643136

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

Submitted genomic138,707,189-138,707,189

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5643136	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	138,707,189	138,707,189
nsv5643136	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	138,391,934	138,391,934

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17151872	insertion	SAMN00006580	Sequencing	Sequence alignment	9,409

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17151872	Submitted genomic		NC_000007.14:g.138 707189_138707190in s142	GRCh38 (hg38)		NC_000007.14	Chr7	138,707,189	138,707,189
nssv17151872	Remapped	Perfect	NC_000007.13:g.138 391934_138391935in s142	GRCh37.p13	First Pass	NC_000007.13	Chr7	138,391,934	138,391,934

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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