A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527193



Internal ID20900554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21711070..21723947hg38UCSC Ensembl
chr18:19291031..19303908hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3812878
hg1912878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527193
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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