A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026746



Internal ID18769277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:66727391..66881929hg38UCSC Ensembl
Innerchr8:67639626..67794164hg19UCSC Ensembl
Innerchr8:67802180..67956718hg18UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38154539
hg19154539
hg18154539
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757283
Samples
Known GenesC8orf44-SGK3, MCMDC2, PTTG3P, SGK3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026746
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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