A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087066



Internal ID21996299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87765204..87765204hg38UCSC Ensembl
chr13:88417459..88417459hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087066
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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