A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378226



Internal ID21035779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168466959..168467193hg38UCSC Ensembl
chr4:169388110..169388344hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115349
Samples
Known GenesDDX60L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378226
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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