A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990333



Internal ID20557373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3044537..3047207hg38UCSC Ensembl
chr11:3065767..3068437hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382671
hg192671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435916
Supporting Variants
Samples
Known GenesCARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990333
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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