A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029567



Internal ID21938910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37582847..37596985hg38UCSC Ensembl
chr11:37604397..37618535hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3814139
hg1914139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029567
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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