A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426106



Internal ID21083659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101922761..101923041hg38UCSC Ensembl
chr8:102934989..102935269hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162043
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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