A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806497



Internal ID21251835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24251434..24251501hg38UCSC Ensembl
chr2:24474303..24474370hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682033
Samples
Known GenesITSN2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806497
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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