A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528352



Internal ID20901713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3676065..3694276hg38UCSC Ensembl
chr20:3656712..3674923hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3818212
hg1918212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202220
Samples
Known GenesADAM33, SIGLEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528352
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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