A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433955



Internal ID21091508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6632917..6698794hg38UCSC Ensembl
chr8:6490438..6556315hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3865878
hg1965878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224030
Samples
Known GenesMCPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433955
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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