A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996558



Internal ID20563598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9940335..9953320hg38UCSC Ensembl
chr11:9961882..9974867hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3812986
hg1912986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437770
Supporting Variants
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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