A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615986



Internal ID16403395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136896406..136900897hg38UCSC Ensembl
Innerchr9:139790858..139795349hg19UCSC Ensembl
Innerchr9:138910679..138915170hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384492
hg194492
hg184492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148338
Samples
Known GenesTRAF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615986
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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