A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523449



Internal ID15104056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15269759..15280318hg38UCSC Ensembl
Innerchr10:15311758..15322317hg19UCSC Ensembl
Innerchr10:15351764..15362323hg18UCSC Ensembl
Innerchr10:15351764..15362323hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3810560
hg1910560
hg1810560
hg1710560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699206
Samples
Known GenesFAM171A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523449
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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