A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109175



Internal ID22018408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34711837..34711837hg38UCSC Ensembl
chr20:33299641..33299641hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620715
Samples
Known GenesTP53INP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109175
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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