A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416827



Internal ID21074380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10358072..10697935hg38UCSC Ensembl
chr8:10215582..10555445hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38339864
hg19339864
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233218
Samples
Known GenesC8orf74, MSRA, PRSS55, RP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416827
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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