A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737373



Internal ID161039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120305090..120310544hg38UCSC Ensembl
chrX:119438945..119444399hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg385455
hg195455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426600
Supporting Variants
Samples
Known GenesTMEM255A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737373
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00145682


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