A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3650336



Internal ID18948617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181015388..181112713hg38UCSC Ensembl
Innerchr5:180442388..180539713hg19UCSC Ensembl
Innerchr5:180374994..180472319hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3897326
hg1997326
hg1897326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028069
Supporting Variants
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)nssv3650336
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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