A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457489



Internal ID21115042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111665515..111673055hg38UCSC Ensembl
chr11:111536239..111543779hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg387541
hg197541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986772
Samples
Known GenesSIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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