A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449906



Internal ID21107459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11272140..11278333hg38UCSC Ensembl
chr11:11293687..11299880hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg386194
hg196194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986816
Samples
Known GenesGALNT18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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