A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995287



Internal ID20562327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94174772..94175243hg38UCSC Ensembl
chr11:93907938..93908409hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471341
Supporting Variants
Samples
Known GenesPANX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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