A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529645



Internal ID20903006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37566776..37569587hg38UCSC Ensembl
chr20:36195178..36197989hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg382812
hg192812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068793
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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