A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531774



Internal ID20905135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38747101..38749200hg38UCSC Ensembl
chr20:37375744..37377843hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202248
Samples
Known GenesACTR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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