A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027665



Internal ID19116884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180972361..181040482hg38UCSC Ensembl
Innerchr5:180399361..180467482hg19UCSC Ensembl
Innerchr5:180331967..180400088hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3868122
hg1968122
hg1868122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5857n100
Supporting Variantsnssv3650326
Samples
Known GenesBTNL3, BTNL9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027665
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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