A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638551



Internal ID21586856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139251281..139251281hg38UCSC Ensembl
chr6:139572418..139572418hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141549
SamplesHG01596
Known GenesTXLNB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638551
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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