A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530361



Internal ID20903722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5994001..6067900hg38UCSC Ensembl
chr20:5974647..6048546hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3873900
hg1973900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203355
Samples
Known GenesCRLS1, LRRN4, MCM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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