A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737095



Internal ID160761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97351659..97353743hg38UCSC Ensembl
chrX:96606658..96608742hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg382085
hg192085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414757
Supporting Variants
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737095
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00843


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