A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426999



Internal ID205913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141954878..141955268hg38UCSC Ensembl
chrX:141042664..141043054hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426999
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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