A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615922



Internal ID21564227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55480383..55480383hg38UCSC Ensembl
chr2:55707519..55707519hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113513
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615922
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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