A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527387



Internal ID303488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35353740..35442000hg38UCSC Ensembl
chr17:33680759..33769019hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3888261
hg1988261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712803
Samples
Known GenesSLFN11, SLFN12, SLFN13
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527387
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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