A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520777



Internal ID20894138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18822355..18828116hg38UCSC Ensembl
chr20:18802999..18808760hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg385762
hg195762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067319
Samples
Known GenesC20orf78
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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