A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519897



Internal ID296238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73171933..73173096hg38UCSC Ensembl
chr17:71168072..71169235hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381164
hg191164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519897
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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