A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565862



Internal ID21514179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135214227..135218827hg38UCSC Ensembl
chr2:135971797..135976397hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg384601
hg194601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109000
SamplesNA19238
Known GenesZRANB3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565862
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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