A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888215



Internal ID22663217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63299216..63308563hg38UCSC Ensembl
chr6:64009121..64018468hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg389348
hg199348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431699
Samples
Known GenesLGSN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888215
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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