A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806235



Internal ID21251573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3240237..3240237hg38UCSC Ensembl
chr2:3244008..3244008hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707766
Samples
Known GenesTSSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806235
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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