A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419009



Internal ID22476879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74203878..74203878hg38UCSC Ensembl
chr5:73499703..73499703hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962055
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419009
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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