A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457397



Internal ID21114950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101486601..101488600hg38UCSC Ensembl
chr11:101357332..101359331hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985577
Samples
Known GenesTRPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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