A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737893



Internal ID161559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148867258..148873939hg38UCSC Ensembl
chrX:147948788..147955469hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386682
hg196682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415069
Supporting Variants
Samples
Known GenesAFF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737893
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00291363


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