A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962055



Internal ID22736995
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 StatusM
Merged Variants
Supporting Variantsnssv17419009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962055
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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