A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367273



Internal ID21024826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25165434..25185601hg38UCSC Ensembl
chr4:25167056..25187223hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3820168
hg1920168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211793
Samples
Known GenesSEPSECS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367273
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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