A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613298



Internal ID16400707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8787733..8800078hg38UCSC Ensembl
Innerchr9:8787733..8800078hg19UCSC Ensembl
Innerchr9:8777733..8790078hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3812346
hg1912346
hg1812346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156233
SamplesHGDP01298
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613298
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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