A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623864



Internal ID21572169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55480387..55480387hg38UCSC Ensembl
chr2:55707523..55707523hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113514
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623864
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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