A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507189



Internal ID20880477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24603691..24607089hg38UCSC Ensembl
chr16:24615012..24618410hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383399
hg193399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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