A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897406



Internal ID22672508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63493606..63499951hg38UCSC Ensembl
chr6:64203511..64209856hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg386346
hg196346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897406
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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