A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363526



Internal ID21021079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25767501..25768900hg38UCSC Ensembl
chr4:25769123..25770522hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114020
Samples
Known GenesSEL1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363526
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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