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dbVar

Database of genomic structural variation

nsv5998651

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:357,409

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: 1086 SVs from 83 studies. See in: genome view

Submitted genomic90,377,354-90,734,762

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5998651	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	90,377,354	90,734,762
nsv5998651	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	91,298,505	91,655,913

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17551423	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17551423	Submitted genomic		NC_000004.12:g.903 77354_90734762dup	GRCh38 (hg38)		NC_000004.12	Chr4	90,377,354	90,734,762
nssv17551423	Remapped	Perfect	NC_000004.11:g.912 98505_91655913dup	GRCh37.p13	First Pass	NC_000004.11	Chr4	91,298,505	91,655,913

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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