A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527211



Internal ID15107818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9910477..9943026hg38UCSC Ensembl
Innerchr4:9912101..9944650hg19UCSC Ensembl
Innerchr4:9521199..9553748hg18UCSC Ensembl
Innerchr4:9588370..9620919hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3832550
hg1932550
hg1832550
hg1732550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703611
Samples
Known GenesSLC2A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527211
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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