A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034658



Internal ID21944001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1486808..1487010hg38UCSC Ensembl
chr11:1508038..1508240hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594976
Samples
Known GenesMOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034658
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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