A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028069



Internal ID19117287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181015388..181112713hg38UCSC Ensembl
Innerchr5:180442388..180539713hg19UCSC Ensembl
Innerchr5:180374994..180472319hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3897326
hg1997326
hg1897326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5859n100
Supporting Variantsnssv3650336
Samples
Known GenesBTNL9, MIR8089
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028069
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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