A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430511



Internal ID21088064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101728097..101730993hg38UCSC Ensembl
chr8:102740325..102743221hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg382897
hg192897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161413
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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