A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740241



Internal ID163907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56236832..56736431hg38UCSC Ensembl
chrX:56263265..56762864hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38499600
hg19499600
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558396
Supporting Variants
Samples
Known GenesKLF8, LOC550643, UBQLN2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740241
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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