A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378448



Internal ID21036001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107390054..107390854hg38UCSC Ensembl
chr4:108311211..108312011hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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