A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649219



Internal ID18947500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176050105..176192510hg38UCSC Ensembl
Innerchr5:175477108..175619513hg19UCSC Ensembl
Innerchr5:175409714..175552119hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38142406
hg19142406
hg18142406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025451
Supporting Variants
Samples
Known GenesFAM153B, LOC100507387, LOC100996385, LOC643201
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649219
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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