A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv790138



Internal ID16084094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:28350789..28442760hg38UCSC Ensembl
Innerchr12:28503722..28595693hg19UCSC Ensembl
Innerchr12:28394989..28486960hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3891972
hg1991972
hg1891972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557877
Supporting Variants
Samples
Known GenesCCDC91
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv790138
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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