A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625271



Internal ID15848807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35060924..35063627hg38UCSC Ensembl
Outerchr22:35456917..35459620hg19UCSC Ensembl
Outerchr22:33786917..33789620hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382704
hg192704
hg182704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512653
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625271
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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