A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366647



Internal ID22592316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83256823..83268098hg38UCSC Ensembl
chr11:82967865..82979140hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3811276
hg1911276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923590
Supporting Variants
Samples
Known GenesCCDC90B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366647
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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