A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432717



Internal ID21090270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107309879..107311244hg38UCSC Ensembl
chr8:108322107..108323472hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381366
hg191366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162097
Samples
Known GenesANGPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432717
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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