A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657931



Internal ID21606236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110154663..110154663hg38UCSC Ensembl
chr13:110807010..110807010hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096208
SamplesHG03486
Known GenesCOL4A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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