A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904520



Internal ID22679697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10734099..10758843hg38UCSC Ensembl
chr6:10734332..10759076hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3824745
hg1924745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421475
Samples
Known GenesTMEM14B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904520
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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