A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475341



Internal ID21132894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124682504..124692565hg38UCSC Ensembl
chr11:124552400..124562461hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3810062
hg1910062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987835
Samples
Known GenesSPA17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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