A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521555



Internal ID20894916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:66538201..66555900hg38UCSC Ensembl
chr18:64205438..64223137hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3817700
hg1917700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3396n223
Supporting Variantsnssv18197572
Samples
Known GenesCDH19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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