A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385536



Internal ID21043089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107931858..107934271hg38UCSC Ensembl
chr4:108853014..108855427hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg382414
hg192414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107666
Samples
Known GenesCYP2U1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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