A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626882



Internal ID21575187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98137976..98137976hg38UCSC Ensembl
chr10:99897733..99897733hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072084
SamplesHG02011
Known GenesR3HCC1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626882
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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