A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340467



Internal ID20998020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222404321..222405048hg38UCSC Ensembl
chr2:223269040..223269767hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340467
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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