A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739160



Internal ID162826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8488069..8488304hg38UCSC Ensembl
chrX:8456110..8456345hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739160
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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