A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704389



Internal ID15094355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144427623..144443060hg38UCSC Ensembl
Innerchr8:145653006..145668443hg19UCSC Ensembl
Innerchr8:145623814..145639251hg18UCSC Ensembl
Innerchr8:145623814..145639251hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3815438
hg1915438
hg1815438
hg1715438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515809
Supporting Variants
Samples
Known GenesLOC100287098, MIR6893, TONSL, VPS28
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704389
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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