A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615183



Internal ID16402592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111214463..111235607hg38UCSC Ensembl
Innerchr9:113976743..113997887hg19UCSC Ensembl
Innerchr9:113016564..113037708hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3821145
hg1921145
hg1821145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12849n54
Supporting Variantsnssv1141224
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615183
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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