A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474872



Internal ID21132425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122939132..122943003hg38UCSC Ensembl
chr11:122809840..122813711hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg383872
hg193872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987653
Samples
Known GenesC11orf63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474872
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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