A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567156



Internal ID21515488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226224544..226225107hg38UCSC Ensembl
chr2:227089260..227089823hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111620
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567156
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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