A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017688



Internal ID18760222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:169114837..169168947hg38UCSC Ensembl
Innerchr5:168541842..168595951hg19UCSC Ensembl
Innerchr5:168474420..168528529hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3854111
hg1954110
hg1854110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649121
Samples
Known GenesSLIT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017688
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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