A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590441



Internal ID16377850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62138804..62220565hg38UCSC Ensembl
Innerchr3:62124478..62206239hg19UCSC Ensembl
Innerchr3:62099518..62181279hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3881762
hg1981762
hg1881762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963556
Samples
Known GenesPTPRG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590441
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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