A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417384



Internal ID196582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137439013..137440320hg38UCSC Ensembl
chrX:136521172..136522479hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417384
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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