A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128802



Internal ID15981988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15590118..15668608hg38UCSC Ensembl
Innerchr9:15590116..15668606hg19UCSC Ensembl
Innerchr9:15580116..15658606hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3878491
hg1978491
hg1878491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613653
Supporting Variants
Samples
Known GenesCCDC171
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1128802
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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