A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517615



Internal ID15444908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68304752..68309476hg38UCSC Ensembl
Innerchr10:70064509..70069233hg19UCSC Ensembl
Innerchr10:69734515..69739239hg18UCSC Ensembl
Innerchr10:69734515..69739239hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384725
hg194725
hg184725
hg174725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652520, nssv670157, nssv684950, nssv673468, nssv682104, nssv666312, nssv661631, nssv675016, nssv660301, nssv688681, nssv683821, nssv686063, nssv664721, nssv658426, nssv661869, nssv670685, nssv654310, nssv686482, nssv657376, nssv679968, nssv687543, nssv658203, nssv693369, nssv655660, nssv680031, nssv681663, nssv682670, nssv653423, nssv677081, nssv663964, nssv690207, nssv676170, nssv674699
Samples
Known GenesPBLD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517615
Frequency
Sample Size2026
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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