A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590638



Internal ID16378047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:73624096..73625489hg38UCSC Ensembl
Innerchr3:73673247..73674640hg19UCSC Ensembl
Innerchr3:73755937..73757330hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381394
hg191394
hg181394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965597
Samples
Known GenesPDZRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590638
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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