A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175416



Internal ID15531702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:4289921..4302638hg38UCSC Ensembl
Innerchr12:4399087..4411804hg19UCSC Ensembl
Innerchr12:4269348..4282065hg18UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3812718
hg1912718
hg1812718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557121
Supporting Variants
SamplesHGDP01191
Known GenesCCND2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175416
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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