A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096511



Internal ID22005744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:116853..116853hg38UCSC Ensembl
chr11:179813..179813hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381925
hg191925
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096511
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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