A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431369



Internal ID21088922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90004435..90018189hg38UCSC Ensembl
chr8:91016663..91030417hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3813755
hg1913755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173676
Samples
Known GenesDECR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431369
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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