A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347779



Internal ID21005332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:30219797..30224802hg38UCSC Ensembl
chr2:30442663..30447668hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg385006
hg195006
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347779
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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