A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736533



Internal ID160199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40862793..40863108hg38UCSC Ensembl
chrX:40722046..40722361hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421180
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736533
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.025297


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