A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496303



Internal ID20869503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89775163..89860298hg38UCSC Ensembl
chr16:89841571..89926706hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3885136
hg1985136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2961n223
Supporting Variantsnssv18179892
Samples
Known GenesFANCA, SPIRE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496303
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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