A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3587371



Internal ID18538966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20135385..20272531hg38UCSC Ensembl
Innerchr22:20122908..20260054hg19UCSC Ensembl
Innerchr22:18502908..18640054hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38137147
hg19137147
hg18137147
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058133
Supporting Variants
Samples
Known GenesLINC00896, LOC284865, LOC388849, MIR1286, RTN4R, ZDHHC8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3587371
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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