A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106396



Internal ID22015629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45389766..45389766hg38UCSC Ensembl
chr20:44018406..44018406hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381368
hg191368
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628590
Samples
Known GenesSYS1-DBNDD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106396
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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