A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649293



Internal ID18600888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179002974..179088195hg38UCSC Ensembl
Innerchr5:178429975..178515196hg19UCSC Ensembl
Innerchr5:178362581..178447802hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3885222
hg1985222
hg1885222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025616
Supporting Variants
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)nssv3649293
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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