A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9126n54



Internal ID22777021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70115421..70215321hg38UCSC Ensembl
chr4:70981138..71081038hg19UCSC Ensembl
chr4:71015727..71115627hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3899901
hg1999901
hg1899901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594644, nsv594645
Samples
Known GenesC4orf40, CSN1S2BP, ODAM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9126n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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