A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968678



Internal ID22743613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38978015..38978015hg38UCSC Ensembl
chr20:37606658..37606658hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399047
Samples
Known GenesDHX35
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968678
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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