A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995286



Internal ID20562326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9417290..9419329hg38UCSC Ensembl
chr11:9438837..9440876hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382040
hg192040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442814
Supporting Variants
Samples
Known GenesIPO7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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