A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905052



Internal ID22680233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157925242..157925966hg38UCSC Ensembl
chr6:158346274..158346998hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424536
Samples
Known GenesSNX9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905052
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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