A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533023



Internal ID308921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4994958..4995801hg38UCSC Ensembl
chr17:4898253..4899096hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38844
hg19844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711022
Samples
Known GenesINCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533023
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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