A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993203



Internal ID62922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22760188..22760188hg38UCSC Ensembl
chr7:22799807..22799807hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5404126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993203
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.358533


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