A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418757



Internal ID21076310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34851948..34858876hg38UCSC Ensembl
chr8:34709466..34716394hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386929
hg196929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418757
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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