A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424502



Internal ID203491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101165040..101166569hg38UCSC Ensembl
chrX:100420029..100421558hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg381530
hg191530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741711
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424502
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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