A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953384



Internal ID22728673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90494372..90494372hg38UCSC Ensembl
chr6:91204091..91204091hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432349
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953384
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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