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dbVar

Database of genomic structural variation

nsv4747449

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:70

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: 115 SVs from 18 studies. See in: genome view

Remapped(Score: Perfect):33,083,097-33,083,166

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4747449	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	33,083,097	33,083,166
nsv4747449	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	33,574,003	33,574,072

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16296301	deletion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16296301	Remapped	Perfect	NC_000019.10:g.330 83097_33083166del	GRCh38.p12	First Pass	NC_000019.10	Chr19	33,083,097	33,083,166
nssv16296301	Submitted genomic		NC_000019.9:g.3357 4003_33574072del	GRCh37 (hg19)		NC_000019.9	Chr19	33,574,003	33,574,072

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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