A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465077



Internal ID21122630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118065072..118067880hg38UCSC Ensembl
chr11:117935787..117938595hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382809
hg192809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987177
Samples
Known GenesTMPRSS4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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