A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524333



Internal ID15451626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123991009..124008704hg38UCSC Ensembl
Innerchr10:125750525..125768220hg19UCSC Ensembl
Innerchr10:125740515..125758210hg18UCSC Ensembl
Innerchr10:125740515..125758210hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3817696
hg1917696
hg1817696
hg1717696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700240
Samples
Known GenesCHST15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524333
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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