A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517469



Internal ID15444762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21494705..21533927hg38UCSC Ensembl
Innerchr10:21783634..21822856hg19UCSC Ensembl
Innerchr10:21823640..21862862hg18UCSC Ensembl
Innerchr10:21823640..21862862hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3839223
hg1939223
hg1839223
hg1739223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684817, nssv689498, nssv677688, nssv658409, nssv664604, nssv652113
Samples
Known GenesCASC10, MIR1915, SKIDA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517469
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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