A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091657



Internal ID22000890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15113143..15113143hg38UCSC Ensembl
chr11:15134689..15134689hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592050
Samples
Known GenesINSC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091657
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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