A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613211



Internal ID21561516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:519924..519924hg38UCSC Ensembl
chr4:513713..513713hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122211
SamplesHG03125
Known GenesPIGG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613211
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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