A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626976



Internal ID21575281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84181050..84181050hg38UCSC Ensembl
chr10:85940806..85940806hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071491
SamplesHG00731
Known GenesC10orf99
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626976
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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