A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655961



Internal ID21604266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71553080..71553080hg38UCSC Ensembl
chr13:72127212..72127212hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094073
SamplesHG02011
Known GenesDACH1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655961
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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