A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561833



Internal ID334801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24142334..24144743hg38UCSC Ensembl
chrX:24160451..24162860hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg382410
hg192410
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561833
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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