A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435199



Internal ID21092752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101891101..101897300hg38UCSC Ensembl
chr8:102903329..102909528hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228532
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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