A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378207



Internal ID21035760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:19752257..19831360hg38UCSC Ensembl
chr5:19752366..19831469hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3879104
hg1979104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215629
Samples
Known GenesCDH18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378207
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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