A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462620



Internal ID21120173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41539699..41610100hg38UCSC Ensembl
chr11:41561249..41631650hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3870402
hg1970402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462620
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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