A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020260



Internal ID19109479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139930370..140083406hg38UCSC Ensembl
Innerchr8:140942614..141093505hg19UCSC Ensembl
Innerchr8:141011796..141162687hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38153037
hg19150892
hg18150892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690073
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)nsv1020260
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer