A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706700



Internal ID21378976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41744475..41744796hg38UCSC Ensembl
chr22:42140479..42140800hg19UCSC 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 Variantsnsv4392838
Supporting Variants
Samples
Known GenesMEI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706700
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.931034


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