A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511143



Internal ID20884469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60520301..60539000hg38UCSC Ensembl
chr16:60554205..60572904hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3818700
hg1918700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2897n223
Supporting Variantsnssv18030533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511143
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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