A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559420



Internal ID332453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:22279298..22640571hg38UCSC Ensembl
chr17:21805904..22139898hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38361274
hg19333995
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712262
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559420
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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