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dbVar

Database of genomic structural variation

nsv4730855

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:130

Publication(s):Quan 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 25 studies. See in: genome view

Remapped(Score: Perfect):88,901,004-88,901,133

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4730855	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	88,901,004	88,901,133
nsv4730855	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	89,444,235	89,444,364

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16272702	deletion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16272702	Remapped	Perfect	NC_000015.10:g.889 01004_88901133del	GRCh38.p12	First Pass	NC_000015.10	Chr15	88,901,004	88,901,133
nssv16272702	Submitted genomic		NC_000015.9:g.8944 4235_89444364del	GRCh37 (hg19)		NC_000015.9	Chr15	89,444,235	89,444,364

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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