A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422900



Internal ID21080453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52261418..52656385hg38UCSC Ensembl
chr8:53173978..53568945hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38394968
hg19394968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7342n223
Supporting Variantsnssv18220116
Samples
Known GenesFAM150A, RB1CC1, ST18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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