A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429800



Internal ID208635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121172412..121172473hg38UCSC Ensembl
chrX:120306266..120306327hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429800
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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