A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871431



Internal ID22646369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:67403004..67409553hg38UCSC Ensembl
chrX:66622846..66629395hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg386550
hg196550
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871431
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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