A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431184



Internal ID21088737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39958055..39960869hg38UCSC Ensembl
chr8:39815574..39818388hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg382815
hg192815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167982
Samples
Known GenesIDO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431184
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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