A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378326



Internal ID21035879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:90646767..90650434hg38UCSC Ensembl
chr4:91567918..91571585hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg383668
hg193668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123181
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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