A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898948



Internal ID22674072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14939974..15044742hg38UCSC Ensembl
chr5:14940083..15044851hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38104769
hg19104769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898948
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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