A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469457



Internal ID21127010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43402101..43403000hg38UCSC Ensembl
chr11:43423651..43424550hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991347
Samples
Known GenesTTC17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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