A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420427



Internal ID21077980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105318001..105320200hg38UCSC Ensembl
chr8:106330229..106332428hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228230
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420427
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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