A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385942



Internal ID21043495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152338001..152339400hg38UCSC Ensembl
chr4:153259153..153260552hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112003
Samples
Known GenesDEAR, FBXW7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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