A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128553



Internal ID15635053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11606348..11716862hg38UCSC Ensembl
Innerchr9:11606348..11716862hg19UCSC Ensembl
Innerchr9:11596348..11706862hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38110515
hg19110515
hg18110515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613433
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1128553
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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