A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420032



Internal ID199148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19926924..19928330hg38UCSC Ensembl
chrX:19945042..19946448hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg381407
hg191407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739548
Samples
Known GenesCXorf23
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420032
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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