A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614213



Internal ID16401622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36872317..36886068hg38UCSC Ensembl
Innerchr9:36872314..36886065hg19UCSC Ensembl
Innerchr9:36862314..36876065hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3813752
hg1913752
hg1813752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176448
SamplesHGDP00602
Known GenesPAX5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614213
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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