A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026351



Internal ID18768883
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 StatusM
Merged Variantsdgv5845n100
Supporting Variantsnssv3649294, nssv3649295
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)nsv1026351
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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