A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526991



Internal ID15454284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:156838512..156856286hg38UCSC Ensembl
Innerchr5:156265523..156283297hg19UCSC Ensembl
Innerchr5:156198101..156215875hg18UCSC Ensembl
Innerchr5:156198101..156215875hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3817775
hg1917775
hg1817775
hg1717775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv358n21
Supporting Variantsnssv703365
Samples
Known GenesPPP1R2P3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526991
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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