A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615535



Internal ID16056258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131269410..131347804hg38UCSC Ensembl
Innerchr9:134144797..134223191hg19UCSC Ensembl
Innerchr9:133134618..133213012hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3878395
hg1978395
hg1878395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176513
SamplesNINDS_119
Known GenesFAM78A, PPAPDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615535
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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