A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737682



Internal ID161348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:143715526..143715750hg38UCSC Ensembl
chrX:142798620..142798844hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556302
Supporting Variants
Samples
Known GenesSPANXN2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737682
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.093506


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