A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057931



Internal ID21967164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66361337..66361337hg38UCSC Ensembl
chrX:65581179..65581179hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg385956
hg195956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057931
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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