A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690073



Internal ID18988354
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 StatusS
Merged Variantsnsv1020260
Supporting Variants
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)nssv3690073
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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