A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344039



Internal ID21001592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231716014..231716066hg38UCSC Ensembl
chr2:232580724..232580776hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344039
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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