A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613359



Internal ID16400768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9904481..10008130hg38UCSC Ensembl
Innerchr9:9904481..10008130hg19UCSC Ensembl
Innerchr9:9894481..9998130hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38103650
hg19103650
hg18103650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126956
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613359
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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