A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055363



Internal ID21964597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120582050..120582050hg38UCSC Ensembl
chrX:119715905..119715905hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055363
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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