A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031522



Internal ID21940865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10585559..10585643hg38UCSC Ensembl
chr11:10607106..10607190hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594949
Samples
Known GenesMRVI1, MRVI1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031522
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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