A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4012799



Internal ID22074430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26231176..26275073hg38UCSC Ensembl
Outerchr22:26231176..26279693hg38UCSC Ensembl
Innerchr22:26627142..26671039hg19UCSC Ensembl
Outerchr22:26627142..26675659hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3848518
hg1948518
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155790
Supporting Variants
Samples
Known GenesSEZ6L
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4012799
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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