A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736606



Internal ID160272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42631992..42632414hg38UCSC Ensembl
chrX:42491244..42491666hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736606
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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