A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878986



Internal ID22653953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46219428..46219487hg38UCSC Ensembl
chrX:46078863..46078922hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878986
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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