A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525997



Internal ID302143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5016526..5017579hg38UCSC Ensembl
chr17:4919821..4920874hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711023
Samples
Known GenesKIF1C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525997
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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