A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966817



Internal ID22741752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6321538..6321538hg38UCSC Ensembl
chr5:6321651..6321651hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414518
Samples
Known GenesFLJ33360
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966817
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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