A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644092



Internal ID21592397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79270598..79270598hg38UCSC Ensembl
chr5:78566421..78566421hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141083
SamplesHG03486
Known GenesJMY
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644092
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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