A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522595



Internal ID15449888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103714255..103726319hg38UCSC Ensembl
Innerchr10:105474013..105486077hg19UCSC Ensembl
Innerchr10:105464003..105476067hg18UCSC Ensembl
Innerchr10:105464003..105476067hg17UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3812065
hg1912065
hg1812065
hg1712065
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705985
Samples
Known GenesSH3PXD2A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522595
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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