A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991041



Internal ID20558081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3989965..3995992hg38UCSC Ensembl
chr11:4011195..4017222hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386028
hg196028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445127
Supporting Variants
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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