A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950654



Internal ID34454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70869767..70889947hg38UCSC Ensembl
chr4:71735484..71755664hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3820181
hg1920181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455151
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950654
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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