A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056925



Internal ID21966161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115015236..115015236hg38UCSC Ensembl
chrX:114249799..114249799hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642634
Samples
Known GenesIL13RA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056925
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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