A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739564



Internal ID163230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20579797..20647636hg38UCSC Ensembl
chrX:20597915..20665754hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3867840
hg1967840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739564
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00228928


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