A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141225



Internal ID15994411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111214463..111240467hg38UCSC Ensembl
Innerchr9:113976743..114002747hg19UCSC Ensembl
Innerchr9:113016564..113042568hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3826005
hg1926005
hg1826005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615184
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141225
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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