A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813344



Internal ID21258682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32663139..32663139hg38UCSC Ensembl
chr6:32630916..32630916hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13696838
Samples
Known GenesHLA-DQB1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813344
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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