A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350791



Internal ID21008344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206065304..206070443hg38UCSC Ensembl
chr2:206930028..206935167hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg385140
hg195140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082939
Samples
Known GenesINO80D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350791
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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