A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524367



Internal ID15104974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6933188..6971563hg38UCSC Ensembl
Innerchr8:6790710..6829085hg19UCSC Ensembl
Innerchr8:6778120..6816495hg18UCSC Ensembl
Innerchr8:6778120..6816495hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3838376
hg1938376
hg1838376
hg1738376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700279
Samples
Known GenesDEFA10P, DEFA4, DEFA8P, DEFA9P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524367
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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