A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031336



Internal ID19120558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113580701..113620891hg38UCSC Ensembl
Innerchr5:112916398..112956588hg19UCSC Ensembl
Innerchr5:112944297..112984487hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3840191
hg1940191
hg1840191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5783n100
Supporting Variantsnssv3647067
Samples
Known GenesYTHDC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031336
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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