A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183467



Internal ID20750507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4452172..4502402hg38UCSC Ensembl
chr11:4473402..4523632hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3850231
hg1950231
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437648
Supporting Variants
Samples
Known GenesOR52K1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183467
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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