A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649463



Internal ID21597768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19008750..19008750hg38UCSC Ensembl
chr13:19582890..19582890hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095856
SamplesHG02587
Known GenesLINC00442
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649463
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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