A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615587



Internal ID21563892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:182984423..182984423hg38UCSC Ensembl
chr2:183849151..183849151hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110655, nssv17110654
SamplesNA24385, HG03371
Known GenesNCKAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615587
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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