A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615689



Internal ID16403098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133685695..133705967hg38UCSC Ensembl
Innerchr9:136550817..136571089hg19UCSC Ensembl
Innerchr9:135540638..135560910hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3820273
hg1920273
hg1820273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176522
SamplesHGDP00788
Known GenesSARDH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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