A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740289



Internal ID163955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57211346..57234457hg38UCSC Ensembl
chrX:57237779..57260890hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3823112
hg1923112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425062
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740289
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000832466


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