A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527372



Internal ID15454665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124890173..124893416hg38UCSC Ensembl
Innerchr8:125902415..125905658hg19UCSC Ensembl
Innerchr8:125971596..125974839hg18UCSC Ensembl
Innerchr8:125971596..125974839hg17UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg383244
hg193244
hg183244
hg173244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703804
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527372
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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