A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877189



Internal ID22652152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68678129..68715411hg38UCSC Ensembl
chr16:68712032..68749314hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3837283
hg1937283
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472651
Samples
Known GenesCDH3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877189
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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