A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559478



Internal ID332511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57592387..57910019hg38UCSC Ensembl
chrX:57618820..57936453hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38317633
hg19317634
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740312
Samples
Known GenesZXDA, ZXDB
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559478
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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