A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3588910



Internal ID18540505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22611045..24001082hg38UCSC Ensembl
Innerchr22:22953515..24344410hg19UCSC Ensembl
Innerchr22:21283515..22674410hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg381390038
hg191390896
hg181390896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066891
Supporting Variants
Samples
Known GenesBCR, C22orf15, C22orf43, CES5AP1, CHCHD10, DDT, DDTL, DERL3, FBXW4P1, GGTLC2, GNAZ, GSTT2, GSTT2B, GSTTP1, GUSBP11, IGLL1, IGLL5, LOC284889, MIF, MIR650, MMP11, POM121L1P, RAB36, RGL4, RTDR1, SLC2A11, SMARCB1, VPREB3, ZDHHC8P1, ZNF70
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3588910
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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