A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993506



Internal ID20560546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67665769..67669269hg38UCSC Ensembl
chr11:67433240..67436740hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383501
hg193501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471472
Supporting Variants
Samples
Known GenesALDH3B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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