A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450119



Internal ID21107672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5169893..5248981hg38UCSC Ensembl
chr11:5191123..5270211hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3879089
hg1979089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv959n223
Supporting Variantsnssv17992183
Samples
Known GenesHBB, HBBP1, HBD, HBG1, OR51V1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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