A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613303



Internal ID16400712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9187539..9225463hg38UCSC Ensembl
Innerchr9:9187539..9225463hg19UCSC Ensembl
Innerchr9:9177539..9215463hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3837925
hg1937925
hg1837925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126897
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613303
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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