A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521808



Internal ID15449101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:107697198..107708493hg38UCSC Ensembl
Innerchr10:109456956..109468251hg19UCSC Ensembl
Innerchr10:109446946..109458241hg18UCSC Ensembl
Innerchr10:109446946..109458241hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3811296
hg1911296
hg1811296
hg1711296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694578
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521808
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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