A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998936



Internal ID18811786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58319306..58399467hg38UCSC Ensembl
Innerchr3:58305033..58385194hg19UCSC Ensembl
Innerchr3:58280073..58360234hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3880162
hg1980162
hg1880162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4748n100
Supporting Variantsnssv3593390
Samples
Known GenesPXK, RPP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998936
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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