A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615505



Internal ID16056228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130264100..130270995hg38UCSC Ensembl
Innerchr9:133026379..133033274hg19UCSC Ensembl
Innerchr9:132066200..132073095hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386896
hg196896
hg186896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145119
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615505
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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