A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383905



Internal ID21041458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53200701..53216900hg38UCSC Ensembl
chr4:54066868..54083067hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3816200
hg1916200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5266n223
Supporting Variantsnssv18117395
Samples
Known GenesSCFD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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