A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459395



Internal ID21116948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126243416..126248386hg38UCSC Ensembl
chr11:126113311..126118281hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg384971
hg194971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987331
Samples
Known GenesFAM118B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459395
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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