A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368083



Internal ID21025636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25152433..25153226hg38UCSC Ensembl
chr4:25154055..25154848hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113393
Samples
Known GenesSEPSECS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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