A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033179



Internal ID18775713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74778792..74835423hg38UCSC Ensembl
Innerchr8:75691027..75747658hg19UCSC Ensembl
Innerchr8:75853582..75910213hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3856632
hg1956632
hg1856632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7241n100
Supporting Variantsnssv3689571
Samples
Known GenesPI15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033179
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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