A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986646



Internal ID20553686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119006635..119007315hg38UCSC Ensembl
chr11:118877345..118878025hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38681
hg19681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463818
Supporting Variants
Samples
Known GenesCCDC84
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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