A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804561



Internal ID21249899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9586595..9586595hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38254
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13696991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804561
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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