A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549433



Internal ID20922595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52772138..52778777hg38UCSC Ensembl
chr20:51388677..51395316hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386640
hg196640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068221
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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