A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459490



Internal ID21117043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73112038..73112740hg38UCSC Ensembl
chr11:72823083..72823785hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992815
Samples
Known GenesFCHSD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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