A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039757



Internal ID21949100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37515034..37534847hg38UCSC Ensembl
chr11:37536584..37556397hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3819814
hg1919814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039757
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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