A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521485



Internal ID297780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68087672..68182474hg38UCSC Ensembl
chr17:66083812..66178615hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3894803
hg1994804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714203
Samples
Known GenesLINC00674
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521485
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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