A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026393



Internal ID21935736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86104417..86105942hg38UCSC Ensembl
chr11:85815459..85816984hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg381526
hg191526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026393
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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