A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051211



Internal ID21960444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:127245444..127245444hg38UCSC Ensembl
chrX:126379427..126379427hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051211
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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