A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156259



Internal ID15525959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17391533..17436664hg38UCSC Ensembl
Innerchr9:17391531..17436662hg19UCSC Ensembl
Innerchr9:17381531..17426662hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3845132
hg1945132
hg1845132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613697
Supporting Variants
SamplesHGDP00005
Known GenesCNTLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156259
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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