A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176321



Internal ID15877840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:83671545..83760224hg38UCSC Ensembl
Innerchr12:84065324..84154003hg19UCSC Ensembl
Innerchr12:82589455..82678134hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3888680
hg1988680
hg1888680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559565
Supporting Variants
SamplesHGDP01053
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176321
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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