A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415420



Internal ID194676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152363422..152363530hg38UCSC Ensembl
chrX:151531894..151532002hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738024
Samples
Known GenesGABRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415420
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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