A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456710



Internal ID21114263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38399234..38404075hg38UCSC Ensembl
chr11:38420784..38425625hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg384842
hg194842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456710
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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