A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3650208



Internal ID18601803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180945156..181015908hg38UCSC Ensembl
Innerchr5:180372156..180442908hg19UCSC Ensembl
Innerchr5:180304762..180375514hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3870753
hg1970753
hg1870753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026762
Supporting Variants
Samples
Known GenesBTNL3, BTNL8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3650208
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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