A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560426



Internal ID16001149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:119989067..119989942hg38UCSC Ensembl
Innerchr12:120426871..120427746hg19UCSC Ensembl
Innerchr12:118911254..118912129hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38876
hg19876
hg18876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2911n54
Supporting Variantsnssv803382
Samples
Known GenesCCDC64
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560426
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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