A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521508



Internal ID15448801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:140228915..140302442hg38UCSC Ensembl
Innerchr8:141239014..141312541hg19UCSC Ensembl
Innerchr8:141308196..141381723hg18UCSC Ensembl
Innerchr8:141308196..141381723hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3873528
hg1973528
hg1873528
hg1773528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698125
Samples
Known GenesTRAPPC9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521508
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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