A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5418698



Internal ID197860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121026782..121034275hg38UCSC Ensembl
chrX:120160636..120168129hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg387494
hg197494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5418698
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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