A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527876



Internal ID15455169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:117000026..117025077hg38UCSC Ensembl
Innerchr8:118012265..118037316hg19UCSC Ensembl
Innerchr8:118081446..118106497hg18UCSC Ensembl
Innerchr8:118081446..118106497hg17UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg3825052
hg1925052
hg1825052
hg1725052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704377
Samples
Known GenesSLC30A8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527876
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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