A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016232



Internal ID19105451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:140102006..140242282hg38UCSC Ensembl
Innerchr8:141112105..141252381hg19UCSC Ensembl
Innerchr8:141181287..141321563hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38140277
hg19140277
hg18140277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757499
Samples
Known GenesTRAPPC9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016232
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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