A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805185



Internal ID21250523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1443704..1443770hg38UCSC Ensembl
chr2:1447476..1447542hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13698210
Samples
Known GenesTPO
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805185
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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