A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475066



Internal ID21132619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34009310..34012142hg38UCSC Ensembl
chr11:34030857..34033689hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382833
hg192833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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