A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416027



Internal ID21073580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28321501..28328900hg38UCSC Ensembl
chr8:28179018..28186417hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166144
Samples
Known GenesPNOC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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