A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510719



Internal ID20884040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60844001..60896800hg38UCSC Ensembl
chr16:60877905..60930704hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3852800
hg1952800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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