A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613344



Internal ID16054067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9803954..9860735hg38UCSC Ensembl
Innerchr9:9803954..9860735hg19UCSC Ensembl
Innerchr9:9793954..9850735hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3856782
hg1956782
hg1856782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12506n54
Supporting Variantsnssv1156238
Samples1780862088_A
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613344
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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