A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026137



Internal ID18768669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:66464185..66495887hg38UCSC Ensembl
Innerchr8:67376420..67408122hg19UCSC Ensembl
Innerchr8:67538974..67570676hg18UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3831703
hg1931703
hg1831703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689479
Samples
Known GenesADHFE1, C8orf46
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026137
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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