A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802227



Internal ID21247565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35564494..35564494hg38UCSC Ensembl
chr20:34152411..34152411hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13708287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802227
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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