A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466973



Internal ID21124526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64974965..64991205hg38UCSC Ensembl
chr11:64742437..64758677hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3816241
hg1916241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177773
Samples
Known GenesBATF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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