A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513698



Internal ID20887045
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 StatusM
Merged Variants
Supporting Variantsnssv18185817
Samples
Known GenesCDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513698
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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