A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101897



Internal ID22011130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4428504..4428504hg38UCSC Ensembl
chr20:4409151..4409151hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101897
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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