A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429789



Internal ID208624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115721550..115738000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3816451
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429789
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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