A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993871



Internal ID63364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22092136..22092187hg38UCSC Ensembl
chr7:22131754..22131805hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993871
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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