A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422080



Internal ID21079633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47555370..47635719hg38UCSC Ensembl
chr8:48467932..48548281hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3880350
hg1980350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167689
Samples
Known GenesSPIDR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422080
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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