A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433870



Internal ID21395872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119819840..119821018hg38UCSC Ensembl
chr3:119538687..119539865hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15746009
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433870
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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