A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030802



Internal ID20597842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61816001..61817100hg38UCSC Ensembl
chr16:61849905..61851004hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506168
Supporting Variants
Samples
Known GenesCDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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