A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347759



Internal ID21005312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203739051..203749908hg38UCSC Ensembl
chr2:204603774..204614631hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg3810858
hg1910858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347759
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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