A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019414



Internal ID18761949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:33398406..33457125hg38UCSC Ensembl
Innerchr8:33255924..33314643hg19UCSC Ensembl
Innerchr8:33375466..33434185hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3858720
hg1958720
hg1858720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685561
Samples
Known GenesFUT10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019414
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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