A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987873



Internal ID20554913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125246373..125248241hg38UCSC Ensembl
chr11:125116269..125118137hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381869
hg191869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469122
Supporting Variants
Samples
Known GenesPKNOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987873
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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