A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543464



Internal ID20916712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51956817..51957354hg38UCSC Ensembl
chr20:50573356..50573893hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068160
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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