A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339933



Internal ID20997486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64114456..64115187hg38UCSC Ensembl
chr2:64341590..64342321hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089288
Samples
Known GenesPELI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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