A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417889



Internal ID197074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148924291..148925544hg38UCSC Ensembl
chrX:148005821..148007074hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381254
hg191254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737895
Samples
Known GenesAFF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417889
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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