A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022892



Internal ID19112109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181015388..181099500hg38UCSC Ensembl
Innerchr5:180442388..180526500hg19UCSC Ensembl
Innerchr5:180374994..180459106hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3884113
hg1984113
hg1884113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5859n100
Supporting Variantsnssv3746757
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)nsv1022892
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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