A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128808



Internal ID15981994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15636262..15727520hg38UCSC Ensembl
Innerchr9:15636260..15727518hg19UCSC Ensembl
Innerchr9:15626260..15717518hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3891259
hg1991259
hg1891259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613658
Supporting Variants
Samples
Known GenesCCDC171
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1128808
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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