A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026069



Internal ID18768601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78782003..79269565hg38UCSC Ensembl
Innerchr8:79694238..80181800hg19UCSC Ensembl
Innerchr8:79856793..80344355hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38487563
hg19487563
hg18487563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689582
Samples
Known GenesIL7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026069
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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