A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086761



Internal ID21995994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130418356..130418356hg38UCSC Ensembl
chr11:130288251..130288251hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601069
Samples
Known GenesADAMTS8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086761
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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