A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513450



Internal ID20886794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8577929..8597442hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3819514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513450
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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