A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040717



Internal ID21950056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149260735..149260735hg38UCSC Ensembl
chrX:148342265..148342265hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040717
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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