A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966585



Internal ID22741520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90749848..90749848hg38UCSC Ensembl
chr9:93512130..93512130hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966585
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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