A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094013



Internal ID22003246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131660197..131660197hg38UCSC Ensembl
chr11:131530091..131530091hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600313
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094013
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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