A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156742



Internal ID15881176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26005489..26112750hg38UCSC Ensembl
Innerchr9:26005487..26112748hg19UCSC Ensembl
Innerchr9:25995487..26102748hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38107262
hg19107262
hg18107262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613923
Supporting Variants
SamplesNINDS_79
Known GenesLOC100506422
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156742
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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