A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970629



Internal ID47746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95706704..95713792hg38UCSC Ensembl
chr5:95042408..95049496hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg387089
hg197089
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469775
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970629
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003435


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