A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141263



Internal ID15647763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114167820..114195678hg38UCSC Ensembl
Innerchr9:116930100..116957958hg19UCSC Ensembl
Innerchr9:115969921..115997779hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3827859
hg1927859
hg1827859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615232
Supporting Variants
Samples
Known GenesCOL27A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141263
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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