A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016726



Internal ID18759261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143251666..143317866hg38UCSC Ensembl
Innerchr8:144333836..144400036hg19UCSC Ensembl
Innerchr8:144405211..144471411hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3866201
hg1966201
hg1866201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690099
Samples
Known GenesGLI4, TOP1MT, ZFP41, ZNF696
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016726
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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