A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557572



Internal ID330667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84846153..84882863hg38UCSC Ensembl
chrX:84101160..84137869hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3836711
hg1936710
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557572
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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