A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509931



Internal ID20883244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9446433..9451323hg38UCSC Ensembl
chr16:9540290..9545180hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg384891
hg194891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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