A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736296



Internal ID159962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27627621..27627750hg38UCSC Ensembl
chrX:27645738..27645867hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736296
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.020762


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