A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644731



Internal ID21593036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27333632..27333632hg38UCSC Ensembl
chr13:27907769..27907769hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094448
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644731
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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