A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737211



Internal ID160877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116975186..117168618hg38UCSC Ensembl
chrX:116109154..116302581hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38193433
hg19193428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423271
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737211
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00312175


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