A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3650308



Internal ID18601903
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 StatusS
Merged Variantsnsv1023609
Supporting Variants
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)nssv3650308
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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