A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992085



Internal ID62172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:435285..462670hg38UCSC Ensembl
chr7:475268..502307hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3827386
hg1927040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464747
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992085
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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