A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390734



Internal ID21048287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104471956..104472438hg38UCSC Ensembl
chr4:105393113..105393595hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106903
Samples
Known GenesCXXC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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