A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033380



Internal ID18775914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181136493..181229128hg38UCSC Ensembl
Innerchr5:180563493..180656128hg19UCSC Ensembl
Innerchr5:180496099..180588734hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3892636
hg1992636
hg1892636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5862n100
Supporting Variantsnssv3650348
Samples
Known GenesLOC102577426, MIR4638, OR2V2, TRIM41, TRIM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033380
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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