A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433028



Internal ID21090581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:865996..962912hg38UCSC Ensembl
chr8:815996..912912hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3896917
hg1996917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223146
Samples
Known GenesERICH1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433028
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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