A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736457



Internal ID160123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38893148..38895750hg38UCSC Ensembl
chrX:38752401..38755003hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg382603
hg192603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736457
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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