A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526059



Internal ID15106666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2848415..2859363hg38UCSC Ensembl
Innerchr4:2850142..2861090hg19UCSC Ensembl
Innerchr4:2819940..2830888hg18UCSC Ensembl
Innerchr4:2887148..2898096hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3810949
hg1910949
hg1810949
hg1710949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702297
Samples
Known GenesADD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526059
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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