A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501927



Internal ID20875166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19292910..19318478hg38UCSC Ensembl
chr16:19304232..19329800hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3825569
hg1925569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028142
Samples
Known GenesCLEC19A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501927
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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