A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527531



Internal ID303629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43225482..43231020hg38UCSC Ensembl
chr17:41377505..41382749hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg385539
hg195245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724565
Samples
Known GenesLINC00854
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527531
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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