A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472803



Internal ID21130356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33801149..33811834hg38UCSC Ensembl
chr11:33822695..33833380hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3810686
hg1910686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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