A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv803386



Internal ID15750656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:119989067..119990058hg38UCSC Ensembl
Innerchr12:120426871..120427862hg19UCSC Ensembl
Innerchr12:118911254..118912245hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38992
hg19992
hg18992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560427
Supporting Variants
Samples
Known GenesCCDC64
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv803386
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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