A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457185



Internal ID21114738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122895911..122899075hg38UCSC Ensembl
chr11:122766619..122769783hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg383165
hg193165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987650
Samples
Known GenesC11orf63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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