A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056040



Internal ID21965274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97185451..97185451hg38UCSC Ensembl
chrX:96440450..96440450hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638511
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056040
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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