A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1032n54



Internal ID22768927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34731710..34865418hg38UCSC Ensembl
chr10:35020638..35154346hg19UCSC Ensembl
chr10:35060644..35194352hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38133709
hg19133709
hg18133709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550395, nsv550393
SamplesHGDP00956, HGDP00886
Known GenesPARD3, PARD3-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1032n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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