A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520704



Internal ID20894065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18697744..18708392hg38UCSC Ensembl
chr20:18678388..18689036hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3810649
hg1910649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067317
Samples
Known GenesDTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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