A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437981



Internal ID21095534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16497287..16558678hg38UCSC Ensembl
chr11:16518834..16580225hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3861392
hg1961392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437981
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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