A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350896



Internal ID21008449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70109668..70114704hg38UCSC Ensembl
chr2:70336800..70341836hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg385037
hg195037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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