A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958869



Internal ID22733926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14174320..14174320hg38UCSC Ensembl
chr3:14215820..14215820hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405612
Samples
Known GenesXPC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958869
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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