A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613786



Internal ID16401195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22610367..22749671hg38UCSC Ensembl
Innerchr9:22610366..22749670hg19UCSC Ensembl
Innerchr9:22600366..22739670hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38139305
hg19139305
hg18139305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1131397
Samples
Known GenesFLJ35282
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613786
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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