A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086915



Internal ID21996148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30909068..30909068hg38UCSC Ensembl
chr11:30930615..30930615hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595361
Samples
Known GenesDCDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086915
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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