A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500918



Internal ID20874148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57298466..57300290hg38UCSC Ensembl
chr16:57332378..57334202hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg381825
hg191825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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