A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3372n54



Internal ID22771267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105567314..105664629hg38UCSC Ensembl
chr13:106219663..106316978hg19UCSC Ensembl
chr13:105017664..105114979hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3897316
hg1997316
hg1897316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563001, nsv563009, nsv563003, nsv563008, nsv563005, nsv563002, nsv563007
SamplesHGDP01001, HGDP01004, HGDP00862, HGDP01012, HGDP01016, HGDP01003, HGDP01015
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3372n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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