A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731536



Internal ID20507456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10585534..10585613hg38UCSC Ensembl
chr11:10607081..10607160hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274344
Samples
Known GenesMRVI1, MRVI1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731536
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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