A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023609



Internal ID18766142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180951876..181021171hg38UCSC Ensembl
Innerchr5:180378876..180448171hg19UCSC Ensembl
Innerchr5:180311482..180380777hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3869296
hg1969296
hg1869296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5851n100
Supporting Variantsnssv3746746, nssv3650308, nssv3650307
Samples
Known GenesBTNL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023609
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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