A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038376



Internal ID21947719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32366328..32366523hg38UCSC Ensembl
chr11:32387874..32388069hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038376
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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