A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469966



Internal ID21127519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129832027..129832331hg38UCSC Ensembl
chr11:129701922..129702226hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987742
Samples
Known GenesTMEM45B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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