A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468397



Internal ID21125950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35826882..35829559hg38UCSC Ensembl
chr11:35848432..35851109hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382678
hg192678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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