A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518567



Internal ID20891928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32005990..32006610hg38UCSC Ensembl
chr20:30593793..30594413hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518567
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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