A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416566



Internal ID21074119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15268085..17187766hg38UCSC Ensembl
chr8:15125594..17045275hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381919682
hg191919682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7281n223
Supporting Variantsnssv18165199
Samples
Known GenesFGF20, MICU3, MSR1, TUSC3, ZDHHC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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