A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739032



Internal ID162698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2592000..2601488hg38UCSC Ensembl
chrX:2510041..2519529hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg389489
hg199489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138627
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739032
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000418498


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