A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039720



Internal ID21949063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61760024..61760090hg38UCSC Ensembl
chr11:61527496..61527562hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582005
Samples
Known GenesMYRF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039720
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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