A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724888



Internal ID148554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60404853..60404904hg38UCSC Ensembl
chr17:58482214..58482265hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539761
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724888
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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