A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457085



Internal ID21114638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73289270..73291723hg38UCSC Ensembl
chr11:73000315..73002768hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382454
hg192454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190523
Samples
Known GenesP2RY6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457085
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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