A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440655



Internal ID21098208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104783726..106005877hg38UCSC Ensembl
chr10:106543484..107765635hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381222152
hg191222152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv882n223
Supporting Variantsnssv18179784
Samples
Known GenesSORCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440655
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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