A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519891



Internal ID15447184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5711774..5726530hg38UCSC Ensembl
Innerchr10:5753737..5768493hg19UCSC Ensembl
Innerchr10:5793743..5808499hg18UCSC Ensembl
Innerchr10:5793743..5808499hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3814757
hg1914757
hg1814757
hg1714757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv36n21
Supporting Variantsnssv697109
Samples
Known GenesFAM208B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519891
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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