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dbVar

Database of genomic structural variation

nsv6046460

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:7,229

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

Submitted genomic1,600,430-1,607,658

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6046460	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	1,600,430	1,607,658
nsv6046460	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	1,600,429	1,607,657

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17621350	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17621350	Submitted genomic		NC_000019.10:g.160 0430_1607658del	GRCh38 (hg38)		NC_000019.10	Chr19	1,600,430	1,607,658
nssv17621350	Remapped	Perfect	NC_000019.9:g.1600 429_1607657del	GRCh37.p13	First Pass	NC_000019.9	Chr19	1,600,429	1,607,657

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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