A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424626



Internal ID203609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22680350..22902910hg38UCSC Ensembl
chrX:22698467..22921027hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38222561
hg19222561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739636
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424626
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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