A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432254



Internal ID21394256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71182072..71185711hg38UCSC Ensembl
chr15:71474411..71478050hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383640
hg193640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv262n172
Supporting Variantsnssv15752946
SamplesMDQ025
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432254
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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