A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034460



Internal ID18776994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15555926..15683272hg38UCSC Ensembl
Innerchr8:15413435..15540781hg19UCSC Ensembl
Innerchr8:15457806..15585152hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38127347
hg19127347
hg18127347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675901
Samples
Known GenesTUSC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034460
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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