A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2807156



Internal ID21252494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226300710..226306454hg38UCSC Ensembl
chr2:227165426..227171170hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg385745
hg195745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2807156
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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