A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615142



Internal ID16402551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107198272..107224798hg38UCSC Ensembl
Innerchr9:109960553..109987079hg19UCSC Ensembl
Innerchr9:109000374..109026900hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3826527
hg1926527
hg1826527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176109
Samples1780854599_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615142
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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