A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543919



Internal ID20917160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55688267..55694606hg38UCSC Ensembl
chr20:54263324..54269662hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386340
hg196339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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