A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640128



Internal ID21588433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139349887..139349887hg38UCSC Ensembl
chr6:139671024..139671024hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg386341
hg196341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150964
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640128
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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