A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423508



Internal ID21081061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11531738..11611041hg38UCSC Ensembl
chr8:11389247..11468550hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3879304
hg1979304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7236n223
Supporting Variantsnssv18220430
Samples
Known GenesBLK, LINC00208
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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