A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508858



Internal ID20882162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54855374..54857101hg38UCSC Ensembl
chr16:54889286..54891013hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg381728
hg191728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508858
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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