A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462948



Internal ID21120501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92549419..92564123hg38UCSC Ensembl
chr11:92282585..92297289hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3814705
hg1914705
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195997
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462948
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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