A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447364



Internal ID21104917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10106923..10192336hg38UCSC Ensembl
chr11:10128470..10213883hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3885414
hg1985414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985546
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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