A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742228



Internal ID165894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125098630..125102451hg38UCSC Ensembl
chrX:124232479..124236300hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg383822
hg193822
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560364
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742228
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.002654


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