A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426040



Internal ID204986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102818372..102818439hg38UCSC Ensembl
chrX:102073300..102073367hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741762
Samples
Known GenesLINC00630
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426040
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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