A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989372



Internal ID20556412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15189261..15192080hg38UCSC Ensembl
chr11:15210807..15213626hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382820
hg192820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447345
Supporting Variants
Samples
Known GenesINSC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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