A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955779



Internal ID22730977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36323092..36323092hg38UCSC Ensembl
chr9:36323089..36323089hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955779
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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