A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6903n54



Internal ID22774798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57362342..57447445hg38UCSC Ensembl
chr2:57589477..57674580hg19UCSC Ensembl
chr2:57442981..57528084hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3885104
hg1985104
hg1885104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582089, nsv582090, nsv582091
Samples1780854219_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6903n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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