A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348921



Internal ID21006474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:192812384..193066889hg38UCSC Ensembl
chr2:193677110..193931615hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38254506
hg19254506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4235n223
Supporting Variantsnssv18081177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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