A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428774



Internal ID21086327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10731691..10735587hg38UCSC Ensembl
chr8:10589201..10593097hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383897
hg193897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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