A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439747



Internal ID21097300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18282231..18289396hg38UCSC Ensembl
chr11:18303778..18310943hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387166
hg197166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988644
Samples
Known GenesHPS5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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