A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027623



Internal ID21936966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59672310..59672381hg38UCSC Ensembl
chr11:59439783..59439854hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027623
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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