A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377406



Internal ID21034959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137523021..137523556hg38UCSC Ensembl
chr4:138444175..138444710hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111427
Samples
Known GenesPCDH18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377406
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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