A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515524



Internal ID20888884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47050002..47054999hg38UCSC Ensembl
chr16:47083913..47088910hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg384998
hg194998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515524
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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