A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443205



Internal ID22501075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101121503..101121558hg38UCSC Ensembl
chrX:100376492..100376547hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884052
Supporting Variants
Samples
Known GenesCENPI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443205
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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