A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397344



Internal ID21054897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:45223301..45229200hg38UCSC Ensembl
chr5:45223403..45229302hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397344
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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