A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634266



Internal ID21582571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71514259..71514259hg38UCSC Ensembl
chr6:72223962..72223962hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154831
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634266
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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