A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461942



Internal ID21119495
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 StatusM
Merged Variants
Supporting Variantsnssv18179354
Samples
Known GenesP2RY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461942
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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