A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028769



Internal ID19117987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18777092..19120358hg38UCSC Ensembl
Innerchr5:18777201..19120467hg19UCSC Ensembl
Innerchr5:18812958..19156224hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38343267
hg19343267
hg18343267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5594n100
Supporting Variantsnssv3635895
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028769
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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