A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806125



Internal ID21251463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230937444..230937444hg38UCSC Ensembl
chr2:231802159..231802159hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806125
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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