A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597837



Internal ID21546456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88461156..88461207hg38UCSC Ensembl
chr16:88527564..88527615hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096479
SamplesNA18534
Known GenesZFPM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597837
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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