A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562045



Internal ID335009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54788017..54825346hg38UCSC Ensembl
chrX:54814450..54851779hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3837330
hg1937330
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740168
Samples
Known GenesITIH6, MAGED2, SNORA11
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562045
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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