A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559893



Internal ID332913
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 StatusM
Merged Variants
Supporting Variantsnssv17737137
Samples
Known GenesH2BFM, H2BFWT, H2BFXP, MIR1256, SLC25A53, TMSB15B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559893
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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