A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872160



Internal ID22647099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68732209..68748492hg38UCSC Ensembl
chr16:68766112..68782395hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3816284
hg1916284
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472656
Samples
Known GenesCDH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872160
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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