A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565272



Internal ID21513584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224296632..224301951hg38UCSC Ensembl
chr2:225161349..225166668hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg385320
hg195320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111753
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565272
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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