A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517445



Internal ID15444738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:128847678..128869053hg38UCSC Ensembl
Innerchr8:129859924..129881299hg19UCSC Ensembl
Innerchr8:129929106..129950481hg18UCSC Ensembl
Innerchr8:129929106..129950481hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3821376
hg1921376
hg1821376
hg1721376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671820, nssv674962, nssv668964, nssv682145, nssv682190, nssv652037, nssv681322
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517445
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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