A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526193



Internal ID15453486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41053821..41054832hg38UCSC Ensembl
Innerchr5:41053923..41054934hg19UCSC Ensembl
Innerchr5:41089680..41090691hg18UCSC Ensembl
Innerchr5:41089680..41090691hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg381012
hg191012
hg181012
hg171012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702455
Samples
Known GenesMROH2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526193
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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