A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648722



Internal ID21597027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34742660..34742660hg38UCSC Ensembl
chr18:32322624..32322624hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101144
SamplesHG03486
Known GenesDTNA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648722
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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