A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497888



Internal ID20871096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83218251..83382451hg38UCSC Ensembl
chr16:83251856..83416056hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38164201
hg19164201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032416
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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