A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994091



Internal ID20561131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65101750..65103072hg38UCSC Ensembl
chr11:64869222..64870544hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472768
Supporting Variants
Samples
Known GenesVPS51
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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