A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016140



Internal ID19105358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:115042063..115141777hg38UCSC Ensembl
Innerchr8:116054292..116154006hg19UCSC Ensembl
Innerchr8:116123468..116223182hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3899715
hg1999715
hg1899715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7299n100
Supporting Variantsnssv3691456
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016140
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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