A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614584



Internal ID21562889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16726442..16726442hg38UCSC Ensembl
chr4:16728065..16728065hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134068
SamplesHG02818
Known GenesLDB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614584
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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