A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964589



Internal ID22739524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87804387..87804387hg38UCSC Ensembl
chr6:88514105..88514105hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964589
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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