A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513973



Internal ID20887322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14324281..14392425hg38UCSC Ensembl
chr16:14418138..14486282hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3868145
hg1968145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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