A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738331



Internal ID20514299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61945681..61961288hg38UCSC Ensembl
chr16:61979585..61995192hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3815608
hg1915608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292560
Samples
Known GenesCDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738331
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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