A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030429



Internal ID21939772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61458620..61462250hg38UCSC Ensembl
chr11:61226092..61229722hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg383631
hg193631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590311
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030429
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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