A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554447



Internal ID327634
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 StatusM
Merged Variants
Supporting Variantsnssv17737372
Samples
Known GenesTMEM255A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554447
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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