A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176330



Internal ID15877119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:86881094..86981207hg38UCSC Ensembl
Innerchr12:87274871..87374984hg19UCSC Ensembl
Innerchr12:85799002..85899115hg18UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg38100114
hg19100114
hg18100114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559696
Supporting Variants
SamplesHGDP00937
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176330
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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