A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647319



Internal ID21595624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99945658..99945658hg38UCSC Ensembl
chr13:100597912..100597912hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096233
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647319
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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