A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802237



Internal ID21247575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:407966..407966hg38UCSC Ensembl
chr20:388610..388610hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13690901, nssv13684239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802237
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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