A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417895



Internal ID22475765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84460887..84491581hg38UCSC Ensembl
chr5:83756705..83787399hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3830695
hg1930695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417895
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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