A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649036



Internal ID21597341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109488954..109488954hg38UCSC Ensembl
chr13:110141301..110141301hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098139, nssv17087052, nssv17098143
SamplesHG00512, HG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649036
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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