A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059078



Internal ID21968311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:50057666..50057666hg38UCSC Ensembl
chrX:49822323..49822323hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381225
hg191225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648607
Samples
Known GenesCLCN5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059078
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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