A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506095



Internal ID20879370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57902149..57903524hg38UCSC Ensembl
chr16:57936053..57937428hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381376
hg191376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029809
Samples
Known GenesCNGB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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