A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5413938



Internal ID193227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107979285..107982902hg38UCSC Ensembl
chrX:107222515..107226132hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg383618
hg193618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741882
Samples
Known GenesTEX13B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5413938
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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