A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521560



Internal ID20894921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11943350..11950325hg38UCSC Ensembl
chr18:11943349..11950324hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg386976
hg196976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521560
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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