A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698210



Internal ID21220062
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 StatusS
Merged Variantsnsv2805185
Supporting Variants
Samples
Known GenesTPO
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698210
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.28125


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