A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688765



Internal ID21210621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102002783..102002783hg38UCSC Ensembl
chr2:102619245..102619245hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804922
Supporting Variants
Samples
Known GenesIL1R2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688765
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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