A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516211



Internal ID20889572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61518701..61524600hg38UCSC Ensembl
chr18:59185934..59191833hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3386n223
Supporting Variantsnssv18186846
Samples
Known GenesCDH20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516211
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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