A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876803



Internal ID22651764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119562435..119562588hg38UCSC Ensembl
chrX:118696398..118696551hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446286
Samples
Known GenesCXorf56
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876803
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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