A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987874



Internal ID20554914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125264553..125266253hg38UCSC Ensembl
chr11:125134449..125136149hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462535
Supporting Variants
Samples
Known GenesPKNOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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