A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471637



Internal ID21129190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44896122..44896924hg38UCSC Ensembl
chr11:44917673..44918475hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193827, nssv17991673
Samples
Known GenesTSPAN18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471637
Frequency
Sample Size19652
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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