A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992201



Internal ID62253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1751843..1764885hg38UCSC Ensembl
chr7:1791479..1804521hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3813043
hg1913043
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992201
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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