A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7993n54



Internal ID19000169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20346736..21111491hg38UCSC Ensembl
chr22:20698139..21465780hg19UCSC Ensembl
chr22:19028139..19795780hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38764756
hg19767642
hg18767642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv588296, nsv588294, nsv588291, nsv588295
Samples
Known GenesAIFM3, BCRP2, CRKL, KLHL22, LOC400891, LZTR1, MED15, P2RX6, P2RX6P, PI4KA, POM121L4P, SCARF2, SERPIND1, SLC7A4, SNAP29, THAP7, THAP7-AS1, TMEM191A, TUBA3FP, ZNF74
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7993n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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