A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517787



Internal ID15445080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3749032..3759221hg38UCSC Ensembl
Innerchr10:3791224..3801413hg19UCSC Ensembl
Innerchr10:3781224..3791413hg18UCSC Ensembl
Innerchr10:3781224..3791413hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3810190
hg1910190
hg1810190
hg1710190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657435, nssv653254, nssv683478, nssv680762, nssv667115, nssv664939, nssv688601, nssv679265, nssv673121, nssv670115, nssv689113, nssv656628, nssv677080, nssv693658, nssv682513, nssv667357, nssv686972, nssv686330, nssv690786, nssv680852, nssv683532, nssv667875, nssv661556
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517787
Frequency
Sample Size2026
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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