A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049185



Internal ID21958419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123550564..123550564hg38UCSC Ensembl
chrX:122684415..122684415hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049185
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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