A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737372



Internal ID161038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120305089..120314624hg38UCSC Ensembl
chrX:119438944..119448479hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg389536
hg199536
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554447
Supporting Variants
Samples
Known GenesTMEM255A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737372
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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