A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462509



Internal ID21120062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78929651..78935393hg38UCSC Ensembl
chr11:78640696..78646438hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385743
hg195743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994212
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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