A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039111



Internal ID21948454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83316525..83316652hg38UCSC Ensembl
chr11:83027568..83027695hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039111
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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