A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536699



Internal ID20910044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49934153..49935065hg38UCSC Ensembl
chr20:48550690..48551602hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536699
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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