A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905151



Internal ID22680334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123601914..123602332hg38UCSC Ensembl
chr6:123923059..123923477hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415526
Samples
Known GenesTRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905151
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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