A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525080



Internal ID15452373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5712648..5724374hg38UCSC Ensembl
Innerchr10:5754611..5766337hg19UCSC Ensembl
Innerchr10:5794617..5806343hg18UCSC Ensembl
Innerchr10:5794617..5806343hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3811727
hg1911727
hg1811727
hg1711727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv36n21
Supporting Variantsnssv701136
Samples
Known GenesFAM208B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525080
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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