A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420971



Internal ID21078524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106789996..107380376hg38UCSC Ensembl
chr8:107802224..108392604hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38590381
hg19590381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217556
Samples
Known GenesANGPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420971
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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