A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014800



Internal ID18757335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164983237..165073353hg38UCSC Ensembl
Innerchr3:164701025..164791141hg19UCSC Ensembl
Innerchr3:166183719..166273835hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3890117
hg1990117
hg1890117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738253
Samples
Known GenesSI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014800
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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