A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614300



Internal ID21562605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84737661..84737661hg38UCSC Ensembl
chr1:85203344..85203344hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066498
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614300
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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