A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv803913



Internal ID15751183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540246..124541491hg38UCSC Ensembl
Innerchr12:125024792..125026037hg19UCSC Ensembl
Innerchr12:123590745..123591990hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381246
hg191246
hg181246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560551
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)nssv803913
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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