A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898673



Internal ID22673792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167171644..167183564hg38UCSC Ensembl
chr5:166598649..166610569hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3811921
hg1911921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898673
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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