A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528071



Internal ID20901432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37786838..37815174hg38UCSC Ensembl
chr20:36415240..36443576hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3828337
hg1928337
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202231
Samples
Known GenesCTNNBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528071
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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