A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473836



Internal ID21131389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60613716..60616324hg38UCSC Ensembl
chr11:60381189..60383797hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382609
hg192609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992652
Samples
Known GenesLINC00301
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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