A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352477



Internal ID21010030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218357259..218358414hg38UCSC Ensembl
chr2:219221982..219223137hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381156
hg191156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085895
Samples
Known GenesC2orf62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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