A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804566



Internal ID21249904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12131937..12131937hg38UCSC Ensembl
chr1:143348598..143348598hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13694837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804566
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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