A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547718



Internal ID20920919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52360528..52379934hg38UCSC Ensembl
chr20:50977067..50996473hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3819407
hg1919407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068188
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547718
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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