A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518541



Internal ID15445834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139276743..139290814hg38UCSC Ensembl
Innerchr8:140288986..140303057hg19UCSC Ensembl
Innerchr8:140358168..140372239hg18UCSC Ensembl
Innerchr8:140358168..140372239hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3814072
hg1914072
hg1814072
hg1714072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695985
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518541
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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