A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680905



Internal ID21202764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41744476..41744797hg38UCSC Ensembl
chr22:42140480..42140801hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804800
Supporting Variants
Samples
Known GenesMEI1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680905
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.84375


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