A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737780



Internal ID161446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146322796..146340748hg38UCSC Ensembl
chrX:145404314..145422266hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3817953
hg1917953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737780
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00395421


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