A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2792822



Internal ID21238160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77267440..77267440hg38UCSC Ensembl
chr12:77661220..77661220hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709100
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2792822
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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