A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554429



Internal ID327617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:90773617..90773808hg38UCSC Ensembl
chrX:90028616..90028807hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554429
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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