A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905311



Internal ID22680496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126362332..126362417hg38UCSC Ensembl
chr6:126683478..126683563hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427009
Samples
Known GenesCENPW
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905311
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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