A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087681



Internal ID21996914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13258372..13258372hg38UCSC Ensembl
chr11:13279919..13279919hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087681
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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