A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958353



Internal ID22733424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31220773..31220773hg38UCSC Ensembl
chr8:31078289..31078289hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958353
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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