A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474092



Internal ID21131645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73569414..73572064hg38UCSC Ensembl
chr11:73280459..73283109hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382651
hg192651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993862
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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