A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532653



Internal ID20906014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39201835..39236202hg38UCSC Ensembl
chr20:37830478..37864845hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3834368
hg1934368
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202252
Samples
Known GenesLOC339568
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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