A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507879



Internal ID20881175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25485493..25494090hg38UCSC Ensembl
chr16:25496814..25505411hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg388598
hg198598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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