A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541107



Internal ID20914393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49991042..49995386hg38UCSC Ensembl
chr20:48607579..48611923hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg384345
hg194345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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