A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985499



Internal ID20552539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102750434..102756983hg38UCSC Ensembl
chr11:102621165..102627714hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg386550
hg196550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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