A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029802



Internal ID19119021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94544731..94566121hg38UCSC Ensembl
Innerchr8:95556959..95578349hg19UCSC Ensembl
Innerchr8:95626135..95647525hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3821391
hg1921391
hg1821391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7272n100
Supporting Variantsnssv3757325
Samples
Known GenesKIAA1429
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029802
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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