A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802398



Internal ID21247736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21305488..21308169hg38UCSC Ensembl
chr20:21286126..21288807hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382682
hg192682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13711146
Samples
Known GenesXRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802398
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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