A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028578



Internal ID21937921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70389900..70393460hg38UCSC Ensembl
chr11:70236006..70239566hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg383561
hg193561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028578
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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