A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510380



Internal ID20883698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83443911..83479594hg38UCSC Ensembl
chr16:83477516..83513199hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3835684
hg1935684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032447
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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