A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392553



Internal ID21050106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43518688..43529514hg38UCSC Ensembl
chr5:43518790..43529616hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3810827
hg1910827
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214118
Samples
Known GenesPAIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392553
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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