A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496513



Internal ID20869716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82840631..82844516hg38UCSC Ensembl
chr16:82874236..82878121hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg383886
hg193886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032355
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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