A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028999



Internal ID21938342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1159347..1159959hg38UCSC Ensembl
chr11:1152974..1153576hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38613
hg19603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028999
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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