A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618196



Internal ID21566501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65357984..65357984hg38UCSC Ensembl
chr2:65585118..65585118hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381186
hg191186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113553
SamplesNA19650
Known GenesSPRED2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618196
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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