A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985540



Internal ID20552580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101032066..101035964hg38UCSC Ensembl
chr11:100902797..100906695hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383899
hg193899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475032
Supporting Variants
Samples
Known GenesPGR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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