A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470187



Internal ID21127740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87547835..87561401hg38UCSC Ensembl
chr11:87258727..87272293hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3813567
hg1913567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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