A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16996108



Internal ID64855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35618959..35618961hg38UCSC Ensembl
chr7:35658569..35658571hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16996108
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.219208


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