A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741539



Internal ID165205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94698951..94704333hg38UCSC Ensembl
chrX:93953950..93959332hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg385383
hg195383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138352
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741539
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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