A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518124



Internal ID15445417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92900376..93018526hg38UCSC Ensembl
Innerchr10:94660133..94778283hg19UCSC Ensembl
Innerchr10:94650113..94768263hg18UCSC Ensembl
Innerchr10:94650113..94768263hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38118151
hg19118151
hg18118151
hg17118151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695542
Samples
Known GenesEXOC6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518124
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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