A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556032



Internal ID329179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38047545..38194006hg38UCSC Ensembl
chrX:37906798..38053259hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38146462
hg19146462
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736429
Samples
Known GenesSRPX, SYTL5
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556032
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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