A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541100



Internal ID20914386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41397100..41397579hg38UCSC Ensembl
chr20:40025740..40026219hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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