A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647180



Internal ID21595485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88461035..88461035hg38UCSC Ensembl
chr16:88527443..88527443hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099045
SamplesHG00731
Known GenesZFPM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647180
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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