A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511363



Internal ID20884690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52932945..52937376hg38UCSC Ensembl
chr16:52966857..52971288hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg384432
hg194432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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