A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031189



Internal ID21940532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134046074..134046165hg38UCSC Ensembl
chr11:133915969..133916060hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031189
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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