A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425005



Internal ID203979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2362419..2386365hg38UCSC Ensembl
chrX:2280460..2304406hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3823947
hg1923947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738995
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425005
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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