A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521406



Internal ID15102013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:149405886..149423248hg38UCSC Ensembl
Innerchr5:148785449..148802811hg19UCSC Ensembl
Innerchr5:148765642..148783004hg18UCSC Ensembl
Innerchr5:148765642..148783004hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3817363
hg1917363
hg1817363
hg1717363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698016
Samples
Known GenesMIR143HG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521406
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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