A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375678



Internal ID21033231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107951272..107951720hg38UCSC Ensembl
chr4:108872428..108872876hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107667
Samples
Known GenesCYP2U1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375678
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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