A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431442



Internal ID21088995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96449701..96455900hg38UCSC Ensembl
chr8:97461929..97468128hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431442
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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