A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523097



Internal ID15103704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:64371134..64382934hg38UCSC Ensembl
Innerchr8:65283691..65295491hg19UCSC Ensembl
Innerchr8:65446245..65458045hg18UCSC Ensembl
Innerchr8:65446245..65458045hg17UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3811801
hg1911801
hg1811801
hg1711801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698789
Samples
Known GenesLINC00966, MIR124-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523097
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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