A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021627



Internal ID21930970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75296956..75303015hg38UCSC Ensembl
chr11:75008000..75014059hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386060
hg196060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593486
Samples
Known GenesARRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021627
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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