A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606880



Internal ID21555185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237088360..237088360hg38UCSC Ensembl
chr2:237997003..237997003hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17112179
SamplesHG03683
Known GenesCOPS8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606880
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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