A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622363



Internal ID21814410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34713013..34713013hg38UCSC Ensembl
chr20:33300817..33300817hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111932
Supporting Variants
Samples
Known GenesTP53INP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622363
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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