A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460179



Internal ID21117732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72978258..72988004hg38UCSC Ensembl
chr11:72689303..72699049hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg389747
hg199747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992810
Samples
Known GenesFCHSD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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