A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176453



Internal ID15854773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77039041..77072900hg38UCSC Ensembl
Innerchr9:79653957..79687816hg19UCSC Ensembl
Innerchr9:78843777..78877636hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3833860
hg1933860
hg1833860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614727
Supporting Variants
Samples1780862311_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176453
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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