A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416280



Internal ID21073833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107906101..107907400hg38UCSC Ensembl
chr8:108918329..108919628hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162159
Samples
Known GenesRSPO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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