A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022700



Internal ID21932043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60435914..60438740hg38UCSC Ensembl
chr11:60203387..60206213hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382827
hg192827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581008
Samples
Known GenesMS4A5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022700
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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