A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176059



Internal ID15853811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31842564..31892859hg38UCSC Ensembl
Innerchr9:31842562..31892857hg19UCSC Ensembl
Innerchr9:31832562..31882857hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3850296
hg1950296
hg1850296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614134
Supporting Variants
Samples1780854449_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176059
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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