A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv804153



Internal ID15751423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540951..124545229hg38UCSC Ensembl
Innerchr12:125025497..125029775hg19UCSC Ensembl
Innerchr12:123591450..123595728hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg384279
hg194279
hg184279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560591
Supporting Variants
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv804153
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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