A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992870



Internal ID62711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21248154..21248154hg38UCSC Ensembl
chr7:21287773..21287773hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992870
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008594


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