A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572216



Internal ID21520602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105464667..105464759hg38UCSC Ensembl
chr8:106476895..106476987hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153450
SamplesHG03486
Known GenesZFPM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572216
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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