A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037184



Internal ID21946527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67401910..67401990hg38UCSC Ensembl
chr11:67169381..67169461hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037184
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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