A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991457



Internal ID20558497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41875503..41875862hg38UCSC Ensembl
chr11:41897053..41897412hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467285
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00176


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