A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346204



Internal ID21003757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199998601..200008100hg38UCSC Ensembl
chr2:200863324..200872823hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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