A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461287



Internal ID21118840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118832522..118835903hg38UCSC Ensembl
chr11:118703231..118706612hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383382
hg193382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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