A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8732n54



Internal ID22776627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173510078..173571809hg38UCSC Ensembl
chr3:173227868..173289599hg19UCSC Ensembl
chr3:174710562..174772293hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3861732
hg1961732
hg1861732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592523, nsv592525, nsv592522, nsv592526, nsv592529
SamplesHGDP01061, HGDP00869, HGDP00875
Known GenesNLGN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8732n54
Frequency
Sample Size17421
Observed Gain44
Observed Loss0
Observed Complex0
Frequencyn/a


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