A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504077



Internal ID20877336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29938097..29948744hg38UCSC Ensembl
chr16:29949418..29960065hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3810648
hg1910648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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