A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524801



Internal ID15105408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127943179..127953306hg38UCSC Ensembl
Innerchr8:128955425..128965552hg19UCSC Ensembl
Innerchr8:129024607..129034734hg18UCSC Ensembl
Innerchr8:129024607..129034734hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3810128
hg1910128
hg1810128
hg1710128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700793
Samples
Known GenesPVT1, TMEM75
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524801
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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