A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156734



Internal ID15880876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15615323..15727520hg38UCSC Ensembl
Innerchr9:15615321..15727518hg19UCSC Ensembl
Innerchr9:15605321..15717518hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38112198
hg19112198
hg18112198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613657
Supporting Variants
SamplesNINDS_42
Known GenesCCDC171
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156734
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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