A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018650



Internal ID18761183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179001742..179088195hg38UCSC Ensembl
Innerchr5:178428743..178515196hg19UCSC Ensembl
Innerchr5:178361349..178447802hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3886454
hg1986454
hg1886454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5845n100
Supporting Variantsnssv3649289, nssv3649291, nssv3649290
Samples
Known GenesZNF354C, ZNF879
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018650
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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