A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456578



Internal ID21114131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80049441..80060773hg38UCSC Ensembl
chr11:79760484..79771816hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3811333
hg1911333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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