A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742539



Internal ID166205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136358749..136359289hg38UCSC Ensembl
chrX:135440908..135441448hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563466
Supporting Variants
Samples
Known GenesGPR112
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742539
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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