A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995336



Internal ID20562376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91995397..92005980hg38UCSC Ensembl
chr11:91728563..91739146hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3810584
hg1910584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459286
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995336
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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