A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8651n54



Internal ID22776546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150762808..150763449hg38UCSC Ensembl
chr3:150480595..150481236hg19UCSC Ensembl
chr3:151963285..151963926hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38642
hg19642
hg18642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592040, nsv592038, nsv592044, nsv592042, nsv592039
Samples
Known GenesSIAH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8651n54
Frequency
Sample Size17421
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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