A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649295



Internal ID18600890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179002974..179108308hg38UCSC Ensembl
Innerchr5:178429975..178535309hg19UCSC Ensembl
Innerchr5:178362581..178467915hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38105335
hg19105335
hg18105335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026351
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)nssv3649295
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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