A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516050



Internal ID22574012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2714915..2774110hg38UCSC Ensembl
chrX:2632956..2692151hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3859196
hg1959196
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970979
Supporting Variants
Samples
Known GenesCD99, XG, XGPY2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516050
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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