A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528923



Internal ID15109530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:149408099..149413630hg38UCSC Ensembl
Innerchr5:148787662..148793193hg19UCSC Ensembl
Innerchr5:148767855..148773386hg18UCSC Ensembl
Innerchr5:148767855..148773386hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg385532
hg195532
hg185532
hg175532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705613
Samples
Known GenesMIR143HG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528923
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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