A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029944



Internal ID19119163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75284726..75321984hg38UCSC Ensembl
Innerchr8:76196961..76234219hg19UCSC Ensembl
Innerchr8:76359516..76396774hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3837259
hg1937259
hg1837259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7242n100
Supporting Variantsnssv3689575, nssv3689574
Samples
Known GenesCASC9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029944
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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