A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039513



Internal ID21948856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44790579..44790633hg38UCSC Ensembl
chr11:44812129..44812183hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583734
Samples
Known GenesTSPAN18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039513
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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