A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746692



Internal ID18698287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180688817..180787853hg38UCSC Ensembl
Innerchr5:180115817..180214853hg19UCSC Ensembl
Innerchr5:180048423..180147459hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3899037
hg1999037
hg1899037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025379
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)nssv3746692
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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