A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv965596



Internal ID16259552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:73624096..73624932hg38UCSC Ensembl
Innerchr3:73673247..73674083hg19UCSC Ensembl
Innerchr3:73755937..73756773hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38837
hg19837
hg18837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590637
Supporting Variants
Samples
Known GenesPDZRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv965596
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer