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dbVar

Database of genomic structural variation

nsv5986156

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:112,085

Publication(s):Wu 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: 296 SVs from 43 studies. See in: genome view

Submitted genomic138,093,063-138,205,147

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5986156	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	138,093,063	138,205,147
nsv5986156	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	138,850,633	138,962,717

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17520715	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17520715	Submitted genomic		NC_000002.12:g.138 093063_138205147du p	GRCh38 (hg38)		NC_000002.12	Chr2	138,093,063	138,205,147
nssv17520715	Remapped	Perfect	NC_000002.11:g.138 850633_138962717du p	GRCh37.p13	First Pass	NC_000002.11	Chr2	138,850,633	138,962,717

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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