A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560429



Internal ID16001152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:119989173..119989942hg38UCSC Ensembl
Innerchr12:120426977..120427746hg19UCSC Ensembl
Innerchr12:118911360..118912129hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38770
hg19770
hg18770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2911n54
Supporting Variantsnssv803388
Samples
Known GenesCCDC64
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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