A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664079



Internal ID21612384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88591957..88591957hg38UCSC Ensembl
chr16:88658365..88658365hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083890
SamplesHG00732
Known GenesZC3H18
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664079
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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