A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506645



Internal ID20879929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85852000..85856273hg38UCSC Ensembl
chr16:85885606..85889879hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg384274
hg194274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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