A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471461



Internal ID21129014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124808783..124811489hg38UCSC Ensembl
chr11:124678679..124681385hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382707
hg192707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987843
Samples
Known GenesLOC100507283
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471461
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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