A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638257



Internal ID21586562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14133787..14133787hg38UCSC Ensembl
chr6:14134018..14134018hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155727
SamplesHG02587
Known GenesCD83
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638257
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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