A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033202



Internal ID19122424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113556160..113610295hg38UCSC Ensembl
Innerchr5:112891857..112945992hg19UCSC Ensembl
Innerchr5:112919756..112973891hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3854136
hg1954136
hg1854136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647062
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)nsv1033202
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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