A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353167



Internal ID21010720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226890824..226891979hg38UCSC Ensembl
chr2:227755540..227756695hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg381156
hg191156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087032
Samples
Known GenesRHBDD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353167
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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