A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366674



Internal ID21024227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3869542..3872549hg38UCSC Ensembl
chr4:3871269..3874276hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383008
hg193008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116026
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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