A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089836



Internal ID21999069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25662694..25662694hg38UCSC Ensembl
chr10:25951623..25951623hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577558
Samples
Known GenesLINC00836
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089836
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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