A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882739



Internal ID22657716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151478982..151496057hg38UCSC Ensembl
chrX:150647454..150664529hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3817076
hg1917076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882739
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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