A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935398



Internal ID22710739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88630013..88630103hg38UCSC Ensembl
chr16:88696421..88696511hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378419
Samples
Known GenesZC3H18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935398
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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