A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185817



Internal ID20752857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61681899..61694114hg38UCSC Ensembl
chr16:61715803..61728018hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3812216
hg1912216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513698
Supporting Variants
Samples
Known GenesCDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185817
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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