A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989641



Internal ID20556681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31283696..31328221hg38UCSC Ensembl
chr11:31305243..31349768hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3844526
hg1944526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437280
Supporting Variants
Samples
Known GenesDCDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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