A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017006



Internal ID19106223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179637432..179659481hg38UCSC Ensembl
Innerchr5:179064433..179086482hg19UCSC Ensembl
Innerchr5:178997039..179019088hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3822050
hg1922050
hg1822050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5848n100
Supporting Variantsnssv3649309, nssv3649310
Samples
Known GenesC5orf60
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017006
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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