A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649547



Internal ID21597852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49579764..49579764hg38UCSC Ensembl
chr18:47106134..47106134hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101655
SamplesHG00732
Known GenesLIPG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649547
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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