A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350242



Internal ID21007795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32326413..32354956hg38UCSC Ensembl
chr2:32551482..32580024hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3828544
hg1928543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350242
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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