A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526922



Internal ID15454215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:51859955..51874231hg38UCSC Ensembl
Innerchr8:52772515..52786791hg19UCSC Ensembl
Innerchr8:52935068..52949344hg18UCSC Ensembl
Innerchr8:52935068..52949344hg17UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3814277
hg1914277
hg1814277
hg1714277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703286
Samples
Known GenesPCMTD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526922
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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