A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805589



Internal ID21250927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144497818..144497867hg38UCSC Ensembl
chr2:145255385..145255434hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13698240
Samples
Known GenesZEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805589
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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