A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059082



Internal ID21968315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11427814..11427814hg38UCSC Ensembl
chrX:11445934..11445934hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643833
Samples
Known GenesARHGAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059082
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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