A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv262n172



Internal ID22814636
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 Variants
Supporting Variantsnsv4432253, nsv4432254
SamplesMDQ010, MDQ025
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv262n172
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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