A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046089



Internal ID21955334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:81430540..81430540hg38UCSC Ensembl
chrX:80686039..80686039hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046089
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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