A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742603



Internal ID166269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138185688..138200687hg38UCSC Ensembl
chrX:137267847..137282846hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3815000
hg1915000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742603
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00291363


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