A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339519



Internal ID20997072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:138299816..138313405hg38UCSC Ensembl
chr2:139057386..139070975hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3813590
hg1913590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339519
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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