A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025012



Internal ID21934355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70126838..70126998hg38UCSC Ensembl
chr11:69972944..69973104hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581672
Samples
Known GenesANO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025012
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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