A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995928



Internal ID64728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54340153..54505546hg38UCSC Ensembl
chr7:54407846..54573239hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38165394
hg19165394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487676
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995928
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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