A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802196



Internal ID21247534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29538967..29539025hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802196
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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