A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101462



Internal ID22010695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38978015..38978015hg38UCSC Ensembl
chr20:37606658..37606658hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621658
Samples
Known GenesDHX35
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101462
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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