A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031566



Internal ID18774100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64737106..64787266hg38UCSC Ensembl
Innerchr5:64032933..64083093hg19UCSC Ensembl
Innerchr5:64068689..64118849hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3850161
hg1950161
hg1850161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3640790
Samples
Known GenesCWC27, SREK1IP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031566
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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