A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515203



Internal ID291688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58100155..58139156hg38UCSC Ensembl
chr17:56177516..56216517hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3839002
hg1939002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515203
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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