A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417896



Internal ID197081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114395198..114411198hg38UCSC Ensembl
chrX:113629651..113645651hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3816001
hg1916001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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