A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613308



Internal ID16400717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9409606..9750139hg38UCSC Ensembl
Innerchr9:9409606..9750139hg19UCSC Ensembl
Innerchr9:9399606..9740139hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38340534
hg19340534
hg18340534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156236
Samples1780862339_A
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613308
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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