A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095871



Internal ID22005104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119009439..119009439hg38UCSC Ensembl
chr11:118880149..118880149hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598398
Samples
Known GenesCCDC84
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095871
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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