A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741371



Internal ID165037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:89778573..89786136hg38UCSC Ensembl
chrX:89033572..89041135hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg387564
hg197564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420589
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741371
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0129032


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