A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv358n21



Internal ID22766550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156838512..156856404hg38UCSC Ensembl
chr5:156265523..156283415hg19UCSC Ensembl
chr5:156198101..156215993hg18UCSC Ensembl
chr5:156198101..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 Variants
Supporting Variantsnsv525058, nsv526991
Samples
Known GenesPPP1R2P3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv358n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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