A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533488



Internal ID309377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58331980..58332155hg38UCSC Ensembl
chr17:56409341..56409516hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713805
Samples
Known GenesBZRAP1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533488
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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