A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503687



Internal ID20876943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57899542..57904273hg38UCSC Ensembl
chr16:57933446..57938177hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384732
hg194732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029808
Samples
Known GenesCNGB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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