A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345576



Internal ID21003129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33912385..33972609hg38UCSC Ensembl
chr2:34137452..34197676hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3860225
hg1960225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3831n223
Supporting Variantsnssv18085980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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