A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661685



Internal ID21609990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60255312..60255312hg38UCSC Ensembl
chr13:60829446..60829446hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088432
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661685
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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