A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562619



Internal ID335566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36973093..37590944hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38617852
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562619
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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