A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610865



Internal ID21559170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:139846061..139846061hg38UCSC Ensembl
chr2:140603630..140603630hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109280
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610865
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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