A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497331



Internal ID20870537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19080078..19088515hg38UCSC Ensembl
chr16:19091400..19099837hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg388438
hg198438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028127
Samples
Known GenesCOQ7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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