A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525058



Internal ID15452351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:156838512..156856404hg38UCSC Ensembl
Innerchr5:156265523..156283415hg19UCSC Ensembl
Innerchr5:156198101..156215993hg18UCSC Ensembl
Innerchr5:156198101..156215993hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3817893
hg1917893
hg1817893
hg1717893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv358n21
Supporting Variantsnssv701107
Samples
Known GenesPPP1R2P3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525058
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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