A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619364



Internal ID21567669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45890269..45890269hg38UCSC Ensembl
chr3:45931761..45931761hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132368, nssv17121663
SamplesHG00731, HG03683
Known GenesCCR9, LZTFL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619364
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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