A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156444



Internal ID15873670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18033946..18166114hg38UCSC Ensembl
Innerchr9:18033944..18166112hg19UCSC Ensembl
Innerchr9:18023944..18156112hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38132169
hg19132169
hg18132169
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613723
Supporting Variants
SamplesHGDP00290
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156444
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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