A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613384



Internal ID16400793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10421687..10495679hg38UCSC Ensembl
Innerchr9:10421687..10495679hg19UCSC Ensembl
Innerchr9:10411687..10485679hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3873993
hg1973993
hg1873993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128508
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613384
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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