A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425298



Internal ID204265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123972320..123973986hg38UCSC Ensembl
chrX:123106170..123107836hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381667
hg191667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737511
Samples
Known GenesSTAG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425298
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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