A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018953



Internal ID18761486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119898140..119942592hg38UCSC Ensembl
Innerchr8:120910380..120954832hg19UCSC Ensembl
Innerchr8:120979561..121024013hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3844453
hg1944453
hg1844453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691470
Samples
Known GenesDEPTOR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018953
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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