A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126929



Internal ID15633429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9801907..9816955hg38UCSC Ensembl
Innerchr9:9801907..9816955hg19UCSC Ensembl
Innerchr9:9791907..9806955hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3815049
hg1915049
hg1815049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613336
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126929
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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