A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030809



Internal ID20597849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61876601..61878400hg38UCSC Ensembl
chr16:61910505..61912304hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501577
Supporting Variants
Samples
Known GenesCDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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