A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419519



Internal ID21077072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33383584..33390034hg38UCSC Ensembl
chr8:33241102..33247552hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386451
hg196451
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229224
Samples
Known GenesFUT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419519
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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