A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101569



Internal ID22010802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41555344..41555344hg38UCSC Ensembl
chr20:40183983..40183983hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631612
Samples
Known GenesCHD6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101569
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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