A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6928n54



Internal ID22774823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77555714..77630638hg38UCSC Ensembl
chr2:77782840..77857764hg19UCSC Ensembl
chr2:77636348..77711272hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3874925
hg1974925
hg1874925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582258, nsv582259
Samples1782681110_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6928n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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