A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467944



Internal ID21125497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79422013..79423348hg38UCSC Ensembl
chr11:79133057..79134392hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381336
hg191336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994230
Samples
Known GenesMIR5579, TENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467944
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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