A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740099



Internal ID163765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37544800..37563837hg38UCSC Ensembl
chrX:37404053..37423090hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3819038
hg1919038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138209
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740099
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00167399


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