A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459014



Internal ID21116567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67466493..67467824hg38UCSC Ensembl
chr11:67233964..67235295hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993490
Samples
Known GenesTMEM134
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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