A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615239



Internal ID16055962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114221790..114237348hg38UCSC Ensembl
Innerchr9:116984070..116999628hg19UCSC Ensembl
Innerchr9:116023891..116039449hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3815559
hg1915559
hg1815559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176473
Samples1798860192_A
Known GenesCOL27A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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