A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619021



Internal ID21567326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151046518..151046518hg38UCSC Ensembl
chr1:151018994..151018994hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060785
SamplesHG03371
Known GenesBNIPL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619021
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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