A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526552



Internal ID15453845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131665346..131695675hg38UCSC Ensembl
Innerchr8:132677593..132707922hg19UCSC Ensembl
Innerchr8:132746775..132777104hg18UCSC Ensembl
Innerchr8:132746775..132777104hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3830330
hg1930330
hg1830330
hg1730330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702866
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526552
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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