A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179354



Internal ID20746394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73211796..73240427hg38UCSC Ensembl
chr11:72922841..72951472hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3828632
hg1928632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461942
Supporting Variants
Samples
Known GenesP2RY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179354
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00051


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