A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024994



Internal ID18767526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179002974..179078166hg38UCSC Ensembl
Innerchr5:178429975..178505167hg19UCSC Ensembl
Innerchr5:178362581..178437773hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3875193
hg1975193
hg1875193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5845n100
Supporting Variantsnssv3649292
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)nsv1024994
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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