A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527309



Internal ID15454602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:115876242..116551294hg38UCSC Ensembl
Innerchr8:116888468..117563532hg19UCSC Ensembl
Innerchr8:116957644..117632713hg18UCSC Ensembl
Innerchr8:116957644..117632713hg17UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38675053
hg19675065
hg18675070
hg17675070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703730
Samples
Known GenesLINC00536, MIR6507
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527309
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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