A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv803923



Internal ID15751193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540246..124541865hg38UCSC Ensembl
Innerchr12:125024792..125026411hg19UCSC Ensembl
Innerchr12:123590745..123592364hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381620
hg191620
hg181620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560554
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)nssv803923
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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