A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094885



Internal ID22004118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116844601..116844601hg38UCSC Ensembl
chr11:116715317..116715317hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607935
Samples
Known GenesSIK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094885
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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