A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428050



Internal ID206931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41909638..41910761hg38UCSC Ensembl
chrX:41768891..41770014hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736587
Samples
Known GenesCASK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428050
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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