A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386661



Internal ID21044214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83299721..83306433hg38UCSC Ensembl
chr4:84220874..84227586hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg386713
hg196713
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214725
Samples
Known GenesHPSE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386661
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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