A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429761



Internal ID208597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107046271..107052529hg38UCSC Ensembl
chrX:106289501..106295759hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg386259
hg196259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741850
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429761
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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