A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649324



Internal ID18600919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180688817..180789254hg38UCSC Ensembl
Innerchr5:180115817..180216254hg19UCSC Ensembl
Innerchr5:180048423..180148860hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38100438
hg19100438
hg18100438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031928
Supporting Variants
Samples
Known GenesOR2Y1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649324
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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