A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516703



Internal ID20890064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12201101..12229400hg38UCSC Ensembl
chr18:12201100..12229399hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3828300
hg1928300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196112
Samples
Known GenesC18orf61
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516703
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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