A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426982



Internal ID205896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154780564..154780756hg38UCSC Ensembl
chrX:154008839..154009031hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738148
Samples
Known GenesMPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426982
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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