A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584078



Internal ID21532612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10813740..10813828hg38UCSC Ensembl
chr2:10953866..10953954hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107478
SamplesHG03486
Known GenesPDIA6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584078
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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