A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607186



Internal ID21555491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220756554..220756554hg38UCSC Ensembl
chr2:221621274..221621274hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111300
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607186
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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