A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614021



Internal ID21562326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4411786..4411786hg38UCSC Ensembl
chr4:4413513..4413513hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128277
SamplesHG03125
Known GenesNSG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614021
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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