A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571325



Internal ID21519702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:94782711..94783068hg38UCSC Ensembl
chr2:95448456..95448813hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115286
SamplesHG00512
Known GenesANKRD20A8P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571325
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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