A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737137



Internal ID160803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103919818..104111796hg38UCSC Ensembl
chrX:103174401..103356487hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38191979
hg19182087
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559893
Supporting Variants
Samples
Known GenesH2BFM, H2BFWT, H2BFXP, MIR1256, SLC25A53, TMSB15B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737137
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.004839


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