A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943115



Internal ID22718559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81636958..81642431hg38UCSC Ensembl
chr16:81670563..81676036hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg385474
hg195474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385124
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943115
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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