A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512199



Internal ID20885530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85511564..85515033hg38UCSC Ensembl
chr16:85545170..85548639hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg383470
hg193470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033390
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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