A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952587



Internal ID22727900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91172509..91172509hg38UCSC Ensembl
chr5:90468326..90468326hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952587
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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