A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647088



Internal ID21595393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8653555..8653555hg38UCSC Ensembl
chr18:8653553..8653553hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103785
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647088
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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