A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621852



Internal ID21570157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66876292..66876292hg38UCSC Ensembl
chr2:67103424..67103424hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114772, nssv17114773
SamplesHG02011, HG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621852
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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