A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419816



Internal ID198939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152167838..152167890hg38UCSC Ensembl
chrX:151336310..151336362hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738015
Samples
Known GenesGABRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419816
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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