A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881159



Internal ID22656133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70941339..70956318hg38UCSC Ensembl
chrX:70161189..70176168hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3814980
hg1914980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881159
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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