A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947145



Internal ID22722647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89438377..89490440hg38UCSC Ensembl
chr16:89504785..89556848hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3852064
hg1952064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384172
Samples
Known GenesANKRD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947145
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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