A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515275



Internal ID20888634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4789515..4792382hg38UCSC Ensembl
chr16:4839516..4842383hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382868
hg192868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029752
Samples
Known GenesSMIM22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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