A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615642



Internal ID16403051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133660184..133669166hg38UCSC Ensembl
Innerchr9:136525306..136534288hg19UCSC Ensembl
Innerchr9:135515127..135524109hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg388983
hg198983
hg188983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12937n54
Supporting Variantsnssv1145450
Samples
Known GenesSARDH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615642
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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