A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806584



Internal ID21251922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84892607..84892607hg38UCSC Ensembl
chr2:85119731..85119731hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806584
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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